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648 lines
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100 KiB
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<div class="search"><div class="search_form"><label for="database" class="offscreen_noflow">Search database</label><select id="database"><optgroup label="Recent"><option value="dbvar" selected="selected">dbVar</option><option value="gap">dbGaP</option><option value="clinvar">ClinVar</option><option value="medgen" class="last" data-ac_dict="medgen_disease_name">MedGen</option></optgroup><optgroup label="All"><option value="gquery">All Databases</option><option value="assembly">Assembly</option><option value="biocollections">Biocollections</option><option value="bioproject">BioProject</option><option value="biosample">BioSample</option><option value="books">Books</option><option value="clinvar">ClinVar</option><option value="cdd">Conserved Domains</option><option value="gap">dbGaP</option><option value="dbvar">dbVar</option><option value="gene">Gene</option><option value="genome">Genome</option><option value="gds">GEO DataSets</option><option value="geoprofiles">GEO Profiles</option><option value="gtr">GTR</option><option value="ipg">Identical Protein Groups</option><option value="medgen" data-ac_dict="medgen_disease_name">MedGen</option><option value="mesh" data-ac_dict="mesh_suggestions">MeSH</option><option value="nlmcatalog">NLM Catalog</option><option value="nuccore">Nucleotide</option><option value="omim">OMIM</option><option value="pmc">PMC</option><option value="protein">Protein</option><option value="proteinclusters">Protein Clusters</option><option value="protfam">Protein Family Models</option><option value="pcassay">PubChem BioAssay</option><option value="pccompound">PubChem Compound</option><option value="pcsubstance">PubChem Substance</option><option value="pubmed" data-ac_dict="pm_related_queries_2">PubMed</option><option value="snp">SNP</option><option value="sra">SRA</option><option value="structure">Structure</option><option value="taxonomy">Taxonomy</option><option value="toolkit">ToolKit</option><option value="toolkitall">ToolKitAll</option><option value="toolkitbookgh">ToolKitBookgh</option></optgroup></select><div class="nowrap"><label for="term" class="offscreen_noflow" accesskey="/">Search term</label><div class="nowrap"><input type="text" name="term" id="term" title="Search dbVar" value=""nstd102"[study] AND "Benign/Likely benign"[Clinical Interpretation]" class="jig-ncbiclearbutton jig-ncbiautocomplete" data-jigconfig="isEnabled:false,disableUrl:'NcbiSearchBarAutoComplCtrl'" autocomplete="off" data-sbconfig="ds:'no',pjs:'yes',afs:'yes'" /></div><button id="search" type="submit" class="button_search nowrap" cmd="go">Search</button></div></div><ul class="searchlinks inline_list"><set></set><li><a name="SaveSearch" title="Click to create an email alert for this search" href="/sites/myncbi/searches/save?db=dbvar&qk=3793" id="SaveSearch">Create alert</a></li><li><a href="/dbvar/advanced">Advanced</a></li><li class="help"><a id="help" class="jig-ncbihelpwindow" target="ncbihelp" name="help" href="/dbvar/content/help/">Help</a></li></ul></div>
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<div class="facet_cont" data-db="dbvar" data-default_grps="fg_ObjectType,fg_Organism,fg_VariantType,fg_MethodType,fg_ClinicalInterpretation,fg_HasClinicalInterpretation,fg_SexofSubject,fg_Origin,fg_StudyType,fg_SubjectPhenotypeStatus" data-sd="db:'dbvar',op:'search',term:'%22nstd102%22%5Bstudy%5D%20AND%20%22Benign%2FLikely%20benign%22%5BClinical%20Interpretation%5D',qk:'3793',linkname:'',idsfromresult:'',extra:''"><ul class="facet" data-filter_id="ObjectType" id="_ObjectType" data-ss="yes" data-bm="yes"><li class="filter_grp "><div class="clearfix"><h3>Object Type</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="variant">Variant</a><span class="fcount">(190)</span></li><li class="fil_val"><a href="#" data-value_id="study">Study</a><span class="fcount">(1)</span></li></ul></li></ul><ul class="facet" data-filter_id="Organism" id="_Organism" data-bm="yes"><li class="filter_grp "><div class="clearfix"><h3>Organism</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="org_human">human</a><span class="fcount">(191)</span></li></ul></li></ul><ul class="facet" data-filter_id="VariantType" id="_VariantType"><li class="filter_grp "><div class="clearfix"><h3>Variant Type</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="variant_copy_number_variation">copy number variation</a><span class="fcount">(191)</span></li><li class="fil_val"><a href="#" data-value_id="variant_complex_chromosomal_rearrangement">complex chromosomal rearrangement</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="variant_complex_substitution">complex substitution</a><span class="fcount">(1)</span></li><li class="more_exp"><a data-value_id="fetch_more_exp" class="fetch_more_exp"></a><ul style="display:none" id="VariantType_more_exp"><li class="fil_val"><a href="#" data-value_id="variant_delins">delins</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="variant_insertion">insertion</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="variant_inversion">inversion</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="variant_tandem_duplication">tandem duplication</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="variant_translocation">translocation</a><span class="fcount">(1)</span></li></ul></li></ul></li></ul><ul class="facet" data-filter_id="MethodType" id="_MethodType"><li class="filter_grp "><div class="clearfix"><h3>Method Type</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="method_multiple">Multiple</a><span class="fcount">(191)</span></li></ul></li></ul><ul class="facet" data-filter_id="ClinicalInterpretation" id="_ClinicalInterpretation"><li class="filter_grp "><div class="clearfix"><h3>Clinical Interpretation</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="clin_benign_likely_benign">Benign/Likely benign</a><span class="fcount">(191)</span></li><li class="fil_val"><a href="#" data-value_id="clin_benign">Benign</a><span class="fcount">(24)</span></li><li class="fil_val"><a href="#" data-value_id="clin_likely_benign">Likely benign</a><span class="fcount">(12)</span></li><li class="more_exp"><a data-value_id="fetch_more_exp" class="fetch_more_exp"></a><ul style="display:none" id="ClinicalInterpretation_more_exp"><li class="fil_val"><a href="#" data-value_id="clin_likely_pathogenic">Likely pathogenic</a><span class="fcount">(2)</span></li><li class="fil_val"><a href="#" data-value_id="clin_pathogenic">Pathogenic</a><span class="fcount">(2)</span></li><li class="fil_val"><a href="#" data-value_id="clin_uncertain_significance">Uncertain significance</a><span class="fcount">(2)</span></li><li class="fil_val"><a href="#" data-value_id="clin_conflicting_data_from_submitters">conflicting data from submitters</a><span class="fcount">(2)</span></li><li class="fil_val"><a href="#" data-value_id="clin_affects">Affects</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_conflicting_interpretations_of_pathogenicity">Conflicting interpretations of pathogenicity</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_pathogenic_likely_pathogenic">Pathogenic/Likely pathogenic</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_pathogenic;_other">Pathogenic; other</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_uncertain_risk_allele">Uncertain risk allele</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_uncertain_significance;_pathogenic_likely_pathogenic">Uncertain significance; Pathogenic/Likely pathogenic</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_association">association</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_drug_response">drug response</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_low_penetrance">low penetrance</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_not_provided">not provided</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_other">other</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_protective">protective</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="clin_risk_factor">risk factor</a><span class="fcount">(1)</span></li></ul></li></ul></li></ul><ul class="facet" data-filter_id="HasClinicalInterpretation" id="_HasClinicalInterpretation"><li class="filter_grp "><div class="clearfix"><h3>Has Clinical Interpretation</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="has_clin_yes">Yes</a><span class="fcount">(191)</span></li></ul></li></ul><ul class="facet" data-filter_id="SexofSubject" id="_SexofSubject"><li class="filter_grp "><div class="clearfix"><h3>Sex of Subject</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="sex_of_subject_none">not reported</a><span class="fcount">(191)</span></li></ul></li></ul><ul class="facet" data-filter_id="Origin" id="_Origin"><li class="filter_grp "><div class="clearfix"><h3>Origin</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="origin_not_provided">not provided</a><span class="fcount">(190)</span></li><li class="fil_val"><a href="#" data-value_id="origin_see_clinvar_for_details">see ClinVar for details</a><span class="fcount">(3)</span></li><li class="fil_val"><a href="#" data-value_id="origin_germline">germline</a><span class="fcount">(2)</span></li><li class="more_exp"><a data-value_id="fetch_more_exp" class="fetch_more_exp"></a><ul style="display:none" id="Origin_more_exp"><li class="fil_val"><a href="#" data-value_id="origin_biparental">biparental</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_de_novo">de novo</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_inherited">inherited</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_maternal">maternal</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_not_applicable">not applicable</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_not_reported">not reported</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_paternal">paternal</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_somatic">somatic</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_tested-inconclusive">tested-inconclusive</a><span class="fcount">(1)</span></li><li class="fil_val"><a href="#" data-value_id="origin_unknown">unknown</a><span class="fcount">(1)</span></li></ul></li></ul></li></ul><ul class="facet" data-filter_id="StudyType" id="_StudyType"><li class="filter_grp "><div class="clearfix"><h3>Study Type</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="study_case-set">Case-Set</a><span class="fcount">(191)</span></li></ul></li></ul><ul class="facet" data-filter_id="SubjectPhenotypeStatus" id="_SubjectPhenotypeStatus"><li class="filter_grp "><div class="clearfix"><h3>Subject Phenotype Status</h3><a href="#" data-value_id="" class="clear clear_hide">Clear</a></div><ul><li class="fil_val"><a href="#" data-value_id="pheno_yes">Yes</a><span class="fcount">(191)</span></li></ul></li></ul><ul class="facet facet_reset"><li><a href="#" data-value_id="reset">Clear all</a></li></ul><ul class="facet_tools"><li><a id="more_filter_groups_link" href="#more_filter_groups" class="jig-ncbipopper" data-jigconfig="triggerPosition: 'middle right', destPosition: 'top left', hasArrow: true, arrowDirection: 'left', closeEvent : 'click', openEvent: 'click', adjustFit: 'autoAdjust', openAnimation: 'none', closeAnimation: 'none', addCloseButton:true, width: '180px'">
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Show additional filters</a></li><div id="more_filter_groups" style="display:none;" class="facets_dialog"><button class="ui-ncbipopper-close-button ui-ncbipopper-close-button-generated ui-state-default ui-corner-all ui-button-text-only ui-ncbibutton ui-ncbibutton-blue" generated="true" role="button" aria-disabled="false"><span class="ui-button-text">x</span></button><h4>Additional filters</h4><ul class="filter_groups_more facet"><li><input type="checkbox" id="fg_ObjectType" /><label for="fg_ObjectType">Object Type</label></li><li><input type="checkbox" id="fg_Organism" /><label for="fg_Organism">Organism</label></li><li><input type="checkbox" id="fg_VariantType" /><label for="fg_VariantType">Variant Type</label></li><li><input type="checkbox" id="fg_MethodType" /><label for="fg_MethodType">Method Type</label></li><li><input type="checkbox" id="fg_ClinicalInterpretation" /><label for="fg_ClinicalInterpretation">Clinical Interpretation</label></li><li><input type="checkbox" id="fg_HasClinicalInterpretation" /><label for="fg_HasClinicalInterpretation">Has Clinical Interpretation</label></li><li><input type="checkbox" id="fg_SexofSubject" /><label for="fg_SexofSubject">Sex of Subject</label></li><li><input type="checkbox" id="fg_Origin" /><label for="fg_Origin">Origin</label></li><li><input type="checkbox" id="fg_StudyType" /><label for="fg_StudyType">Study Type</label></li><li><input type="checkbox" id="fg_SubjectPhenotypeStatus" /><label for="fg_SubjectPhenotypeStatus">Subject Phenotype Status</label></li><li><input id="fg_field_search" type="checkbox" /><label for="fg_field_search">Search fields</label></li></ul><div class="actions clearfix"><button class="filter_groups_more_apply jig-ncbibutton primary-action" id="filter_groups_apply" data-jigconfig="'color': 'ui-ncbibutton-blue'">Show</button></div></div></ul><input name="EntrezSystem2.PEntrez.Dbvar.dbVar_Facets.FacetsUrlFrag" sid="1" type="hidden" value="filters=" /><input name="EntrezSystem2.PEntrez.Dbvar.dbVar_Facets.FacetSubmitted" sid="1" type="hidden" value="false" /><input name="EntrezSystem2.PEntrez.Dbvar.dbVar_Facets.BMFacets" sid="1" type="hidden" value="" /></div>
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<div class="jig-ncbitabs ui-tabs ui-widget ui-widget-content ui-corner-all" id="entrezDetailsTabmenu"><input name="EntrezSystem2.PEntrez.Dbvar.dbVar_Entrez_ResultsPanel.dbVar_Entrez_TabularDocSum.CurrFilter" sid="1" type="hidden" value="variant" /><ul class="ui-tabs-nav ui-helper-reset ui-helper-clearfix ui-widget-header ui-corner-all"></ul><div id="studiestab" class="ui-tabs-panel ui-widget-content ui-corner-bottom ui-tabs-hide">loading data ...</div><div id="varianttab" class="ui-tabs-panel ui-widget-content ui-corner-bottom"><div><h3>Number of Variants: 20</h3><div class="ui-ncbigrid-outer-div"><div class="ui-ncbigrid-inner-div"><table class="jig-ncbigrid details" id="variantdetails" data-jigconfig="isPagable: false, isSortable: false, columnTypes: ['str','str', 'str', 'num', 'str', 'str','num']"><thead><tr><th>Variant Region ID</th><th>Type</th><th>Number of Variant Calls</th><th>Study ID</th><th>Organism</th><th>Clinical Assertion</th><th>Location</th><th>Genes in region</th></tr></thead><tbody><tr><td><a href="/dbvar/variants/nsv3921061" title="Link to Variant Accession nsv3921061">nsv3921061</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39210612" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=92165654.5&to=92257473.5&studies=nstd102&variant=nsv3921061" id="nsv39210612">GRCh37 chr13: 92,173,306-92,249,821</a>
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, <a class="genomebrowser" name="nsv39210614" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=90963655.5&to=91055474.5&studies=nstd102&variant=nsv3921061" id="nsv39210614">NCBI36 chr13: 90,971,307-91,047,822</a>
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, <a class="genomebrowser" name="nsv39210616" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=91513400.5&to=91605219.5&studies=nstd102&variant=nsv3921061" id="nsv39210616">GRCh38 chr13: 91,521,052-91,597,567</a>
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</td><td class="genename">GPC5</td></tr><tr><td><a href="/dbvar/variants/nsv3922208" title="Link to Variant Accession nsv3922208">nsv3922208</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39222082" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=16087534.6&to=16171144.4&studies=nstd102&variant=nsv3922208" id="nsv39222082">GRCh38 chr8: 16,094,502-16,164,176</a>
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, <a class="genomebrowser" name="nsv39222084" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=15989414.6&to=16073024.4&studies=nstd102&variant=nsv3922208" id="nsv39222084">NCBI36 chr8: 15,996,382-16,066,056</a>
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, <a class="genomebrowser" name="nsv39222086" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=15945043.6&to=16028653.4&studies=nstd102&variant=nsv3922208" id="nsv39222086">GRCh37 chr8: 15,952,011-16,021,685</a>
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</td><td class="genename">MSR1</td></tr><tr><td><a href="/dbvar/variants/nsv3895487" title="Link to Variant Accession nsv3895487">nsv3895487</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38954872" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=2468822.3&to=2546639.7&studies=nstd102&variant=nsv3895487" id="nsv38954872">GRCh38 chr3: 2,475,307-2,540,154</a>
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, <a class="genomebrowser" name="nsv38954874" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=2510506.3&to=2588323.7&studies=nstd102&variant=nsv3895487" id="nsv38954874">GRCh37 chr3: 2,516,991-2,581,838</a>
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, <a class="genomebrowser" name="nsv38954876" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=2485506.3&to=2563323.7&studies=nstd102&variant=nsv3895487" id="nsv38954876">NCBI36 chr3: 2,491,991-2,556,838</a>
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</td><td class="genename">CNTN4</td></tr><tr><td><a href="/dbvar/variants/nsv3916025" title="Link to Variant Accession nsv3916025">nsv3916025</a></td><td>copy number variation</td><td>3</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign, Likely benign</td><td>
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<a class="genomebrowser" name="nsv39160252" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=57049515&to=57089056&studies=nstd102&variant=nsv3916025" id="nsv39160252">GRCh38 chr6: 57,052,810-57,085,760</a>
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, <a class="genomebrowser" name="nsv39160254" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=56914313&to=56953854&studies=nstd102&variant=nsv3916025" id="nsv39160254">GRCh37 chr6: 56,917,608-56,950,558</a>
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</td><td class="genename">KIAA1586</td></tr><tr><td><a href="/dbvar/variants/nsv3894794" title="Link to Variant Accession nsv3894794">nsv3894794</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38947942" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=142828403.9&to=142837562.1&studies=nstd102&variant=nsv3894794" id="nsv38947942">GRCh37 chr7: 142,829,167-142,836,798</a>
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, <a class="genomebrowser" name="nsv38947944" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=143131310.9&to=143140469.1&studies=nstd102&variant=nsv3894794" id="nsv38947944">GRCh38.p12 chr7: 143,132,074-143,139,705</a>
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</td><td class="genename">PIP</td></tr><tr><td><a href="/dbvar/variants/nsv3917152" title="Link to Variant Accession nsv3917152">nsv3917152</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39171522" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=100966133.2&to=101140899.8&studies=nstd102&variant=nsv3917152" id="nsv39171522">GRCh37 chr7: 100,980,697-101,126,335</a>
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, <a class="genomebrowser" name="nsv39171524" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=100752853.2&to=100927619.8&studies=nstd102&variant=nsv3917152" id="nsv39171524">NCBI36 chr7: 100,767,417-100,913,055</a>
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, <a class="genomebrowser" name="nsv39171526" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=101322852.2&to=101497618.8&studies=nstd102&variant=nsv3917152" id="nsv39171526">GRCh38 chr7: 101,337,416-101,483,054</a>
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</td><td class="genename">COL26A1</td></tr><tr><td><a href="/dbvar/variants/nsv3887282" title="Link to Variant Accession nsv3887282">nsv3887282</a></td><td>copy number variation</td><td>2</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38872822" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=101587031.8&to=101703111.2&studies=nstd102&variant=nsv3887282" id="nsv38872822">GRCh37 chrX: 101,596,705-101,693,437</a>
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, <a class="genomebrowser" name="nsv38872824" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=102332108.6&to=102448190.4&studies=nstd102&variant=nsv3887282" id="nsv38872824">GRCh38.p12 chrX: 102,341,782-102,438,516</a>
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</td><td class="genename">NXF2B</td></tr><tr><td><a href="/dbvar/variants/nsv3922421" title="Link to Variant Accession nsv3922421">nsv3922421</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39224212" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=47516379.5&to=47591410.5&studies=nstd102&variant=nsv3922421" id="nsv39224212">GRCh38 chr17: 47,522,632-47,585,157</a>
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, <a class="genomebrowser" name="nsv39224214" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=45593745.5&to=45668776.5&studies=nstd102&variant=nsv3922421" id="nsv39224214">GRCh37 chr17: 45,599,998-45,662,523</a>
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, <a class="genomebrowser" name="nsv39224216" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=42948744.5&to=43023775.5&studies=nstd102&variant=nsv3922421" id="nsv39224216">NCBI36 chr17: 42,954,997-43,017,522</a>
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</td><td class="genename">NPEPPS</td></tr><tr><td><a href="/dbvar/variants/nsv3914128" title="Link to Variant Accession nsv3914128">nsv3914128</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39141282" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=79332129.9&to=79398720.1&studies=nstd102&variant=nsv3914128" id="nsv39141282">GRCh37 chr7: 79,337,679-79,393,170</a>
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, <a class="genomebrowser" name="nsv39141284" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=79170065.9&to=79236656.1&studies=nstd102&variant=nsv3914128" id="nsv39141284">NCBI36 chr7: 79,175,615-79,231,106</a>
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, <a class="genomebrowser" name="nsv39141286" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=79702813.9&to=79769404.1&studies=nstd102&variant=nsv3914128" id="nsv39141286">GRCh38 chr7: 79,708,363-79,763,854</a>
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</td><td class="genename">LOC105375370</td></tr><tr><td><a href="/dbvar/variants/nsv3913744" title="Link to Variant Accession nsv3913744">nsv3913744</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39137442" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=119028757.8&to=119086157.2&studies=nstd102&variant=nsv3913744" id="nsv39137442">GRCh38 chr3: 119,033,541-119,081,373</a>
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, <a class="genomebrowser" name="nsv39137444" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=118747604.8&to=118805004.2&studies=nstd102&variant=nsv3913744" id="nsv39137444">GRCh37 chr3: 118,752,388-118,800,220</a>
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, <a class="genomebrowser" name="nsv39137446" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=120230294.8&to=120287694.2&studies=nstd102&variant=nsv3913744" id="nsv39137446">NCBI36 chr3: 120,235,078-120,282,910</a>
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</td><td class="genename">IGSF11</td></tr><tr><td><a href="/dbvar/variants/nsv3911314" title="Link to Variant Accession nsv3911314">nsv3911314</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39113142" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=3980.8&to=61020.2&studies=nstd102&variant=nsv3911314" id="nsv39113142">NCBI36 chr20: 8,734-56,266</a>
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, <a class="genomebrowser" name="nsv39113144" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=75339.8&to=132379.2&studies=nstd102&variant=nsv3911314" id="nsv39113144">GRCh38 chr20: 80,093-127,625</a>
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, <a class="genomebrowser" name="nsv39113146" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=55980.8&to=113020.2&studies=nstd102&variant=nsv3911314" id="nsv39113146">GRCh37 chr20: 60,734-108,266</a>
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</td><td class="genename">DEFB125</td></tr><tr><td><a href="/dbvar/variants/nsv3923673" title="Link to Variant Accession nsv3923673">nsv3923673</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39236732" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=67419.7&to=121340.3&studies=nstd102&variant=nsv3923673" id="nsv39236732">GRCh37 chr5: 71,913-116,846</a>
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, <a class="genomebrowser" name="nsv39236734" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=120419.7&to=174340.3&studies=nstd102&variant=nsv3923673" id="nsv39236734">NCBI36 chr5: 124,913-169,846</a>
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, <a class="genomebrowser" name="nsv39236736" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=67304.7&to=121225.3&studies=nstd102&variant=nsv3923673" id="nsv39236736">GRCh38 chr5: 71,798-116,731</a>
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</td><td class="genename">PLEKHG4B</td></tr><tr><td><a href="/dbvar/variants/nsv3917146" title="Link to Variant Accession nsv3917146">nsv3917146</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39171462" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=73593056.3&to=73639505.7&studies=nstd102&variant=nsv3917146" id="nsv39171462">GRCh37 chr8: 73,596,927-73,635,634</a>
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, <a class="genomebrowser" name="nsv39171464" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=72680821.3&to=72727270.7&studies=nstd102&variant=nsv3917146" id="nsv39171464">GRCh38 chr8: 72,684,692-72,723,399</a>
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, <a class="genomebrowser" name="nsv39171466" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=73755610.3&to=73802059.7&studies=nstd102&variant=nsv3917146" id="nsv39171466">NCBI36 chr8: 73,759,481-73,798,188</a>
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</td><td class="genename">KCNB2</td></tr><tr><td><a href="/dbvar/variants/nsv3890190" title="Link to Variant Accession nsv3890190">nsv3890190</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38901902" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=145155.8&to=179695.2&studies=nstd102&variant=nsv3890190" id="nsv38901902">GRCh37 chr12: 148,034-176,816</a>
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, <a class="genomebrowser" name="nsv38901904" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=30678&to=64483&studies=nstd102&variant=nsv3890190" id="nsv38901904">GRCh38.p12 chr12|NW_003571049.1: 33,495-61,665</a>
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, <a class="genomebrowser" name="nsv38901906" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=43549&to=69842&studies=nstd102&variant=nsv3890190" id="nsv38901906">GRCh38.p12 chr12: 45,740-67,650</a>
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</td><td class="genename">IQSEC3</td></tr><tr><td><a href="/dbvar/variants/nsv3916632" title="Link to Variant Accession nsv3916632">nsv3916632</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39166322" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=16784214.8&to=16811674.2&studies=nstd102&variant=nsv3916632" id="nsv39166322">GRCh38 chr22: 16,786,503-16,809,385</a>
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, <a class="genomebrowser" name="nsv39166324" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=17265104.8&to=17292564.2&studies=nstd102&variant=nsv3916632" id="nsv39166324">GRCh37 chr22: 17,267,393-17,290,275</a>
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, <a class="genomebrowser" name="nsv39166326" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=15645104.8&to=15672564.2&studies=nstd102&variant=nsv3916632" id="nsv39166326">NCBI36 chr22: 15,647,393-15,670,275</a>
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</td><td class="genename">XKR3</td></tr><tr><td><a href="/dbvar/variants/nsv3921091" title="Link to Variant Accession nsv3921091">nsv3921091</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39210912" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=118776527.1&to=118802374.9&studies=nstd102&variant=nsv3921091" id="nsv39210912">GRCh37 chr3: 118,778,681-118,800,220</a>
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, <a class="genomebrowser" name="nsv39210914" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=120259217.1&to=120285064.9&studies=nstd102&variant=nsv3921091" id="nsv39210914">NCBI36 chr3: 120,261,371-120,282,910</a>
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, <a class="genomebrowser" name="nsv39210916" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=119057680.1&to=119083527.9&studies=nstd102&variant=nsv3921091" id="nsv39210916">GRCh38 chr3: 119,059,834-119,081,373</a>
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</td><td class="genename">IGSF11</td></tr><tr><td><a href="/dbvar/variants/nsv3871234" title="Link to Variant Accession nsv3871234">nsv3871234</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38712342" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=241554795.6&to=241580637.4&studies=nstd102&variant=nsv3871234" id="nsv38712342">GRCh37 chr2: 241,556,949-241,578,483</a>
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, <a class="genomebrowser" name="nsv38712344" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=240615378.6&to=240641220.4&studies=nstd102&variant=nsv3871234" id="nsv38712344">GRCh38.p12 chr2: 240,617,532-240,639,066</a>
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</td><td class="genename">GPR35</td></tr><tr><td><a href="/dbvar/variants/nsv3892428" title="Link to Variant Accession nsv3892428">nsv3892428</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38924282" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=42224533.3&to=42246670.7&studies=nstd102&variant=nsv3892428" id="nsv38924282">GRCh37 chr7: 42,226,378-42,244,825</a>
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, <a class="genomebrowser" name="nsv38924284" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=42184934.3&to=42207071.7&studies=nstd102&variant=nsv3892428" id="nsv38924284">GRCh38.p12 chr7: 42,186,779-42,205,226</a>
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</td><td class="genename">GLI3</td></tr><tr><td><a href="/dbvar/variants/nsv3894347" title="Link to Variant Accession nsv3894347">nsv3894347</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv38943472" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=86518219.1&to=86538426.9&studies=nstd102&variant=nsv3894347" id="nsv38943472">GRCh37 chr16: 86,519,903-86,536,742</a>
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, <a class="genomebrowser" name="nsv38943474" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=86484613.1&to=86504820.9&studies=nstd102&variant=nsv3894347" id="nsv38943474">GRCh38.p12 chr16: 86,486,297-86,503,136</a>
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</td><td class="genename">FENDRR</td></tr><tr><td><a href="/dbvar/variants/nsv3902711" title="Link to Variant Accession nsv3902711">nsv3902711</a></td><td>copy number variation</td><td>1</td><td><a href="/dbvar/studies/nstd102" title="Link to Study Accession nstd102">nstd102</a></td><td>human</td><td>Benign/Likely benign</td><td>
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<a class="genomebrowser" name="nsv39027112" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=49365577.9&to=49384504.1&studies=nstd102&variant=nsv3902711" id="nsv39027112">GRCh37 chr10: 49,367,155-49,382,926</a>
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, <a class="genomebrowser" name="nsv39027114" href="/dbvar/browse/org/?taxid=&assm=&chr=&from=48157534.9&to=48176461.1&studies=nstd102&variant=nsv3902711" id="nsv39027114">GRCh38.p12 chr10: 48,159,112-48,174,883</a>
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</td><td class="genename">FRMPD2</td></tr></tbody></table></div></div></div></div></div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67d206daa68b6b5afce36185">"nstd102"[study] AND "Benign/Likely benign"[Clinical Interpretati... <span class="number">(191)</span></a>
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<div class="ralinkpop offscreen_noflow">"nstd102"[study] AND "Benign/Likely benign"[Clinical Interpretation]<div class="brieflinkpopdesc">Search</div></div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67d2033384f3725e59848760">C4014803[trait identifier] AND "Translational Medicine Institute,... <span class="number">(1)</span></a>
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<div class="ralinkpop offscreen_noflow">C4014803[trait identifier] AND "Translational Medicine Institute, Shanxi Medical University"[submitter]<div class="brieflinkpopdesc">Search</div></div>
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<div class="tertiary">ClinVar</div>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67d20332f4a390645e86b25f">"Translational Medicine Institute, Shanxi Medical University"[sub... <span class="number">(1)</span></a>
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