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{"id":12497,"date":"2023-11-28T12:01:12","date_gmt":"2023-11-28T17:01:12","guid":{"rendered":"https:\/\/ncbiinsights.ncbi.nlm.nih.gov\/?p=12497"},"modified":"2023-11-28T12:01:12","modified_gmt":"2023-11-28T17:01:12","slug":"updates-clinvar-website","status":"publish","type":"post","link":"https:\/\/ncbiinsights.ncbi.nlm.nih.gov\/2023\/11\/28\/updates-clinvar-website\/","title":{"rendered":"Coming Soon! Updates to the ClinVar Website"},"content":{"rendered":"<p>In order to support the inclusion of submitted <a href=\"https:\/\/ncbiinsights.ncbi.nlm.nih.gov\/2023\/02\/01\/clinvar-support-for-somatic-data\/?utm_source=referral+&utm_medium=ncbi_insights&utm_campaign=clinvar-updates-20231128\">somatic variation data<\/a>, we are updating the <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/clinvar\/?utm_source=referral+&utm_medium=ncbi_insights&utm_campaign=clinvar-updates-20231128\">ClinVar<\/a> website. In early 2024, you will begin to see some changes.<\/p>\n<h5>What will change?<\/h5>\n<p>Variant (VCV) record pages will have an updated look and feel:<\/p>\n<ul>\n<li><span style=\"font-size: 17px;\">Simpler layout with no tabs<\/span><\/li>\n<li><span style=\"font-size: 17px;\">New sections will display somatic classifications<\/span>\n<ul>\n<li><span style=\"font-size: 17px;\">Summary section will be divided into germline classification and display the two types of classifications for somatic variants – somatic clinical impact and oncogenicity<\/span><\/li>\n<li><span style=\"font-size: 17px;\">Sections for conditions, submitted records, functional evidence, and citations will be provided for both germline and somatic classifications<\/span><\/li>\n<li><span style=\"font-size: 17px;\">A toggle will allow you to select and show just information pertaining to germline or somatic data\u00a0<\/span><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p><!--more--><\/p>\n<p>In addition, on the ClinVar search results page, you will be able to filter the list of results to display only those variants with either germline or somatic classifications.<\/p>\n<p>Preview sample snapshots of upcoming changes on <a href=\"https:\/\/github.com\/ncbi\/clinvar\/tree\/master\/sample_web_snapshots\">Github<\/a>!<\/p>\n<h5>Stay up to date<\/h5>\n<p>Follow us on social\u00a0<a href=\"https:\/\/twitter.com\/ncbi\">@NCBI<\/a>\u202fand\u202f<a href=\"https:\/\/public.govdelivery.com\/accounts\/USNLMOCPL\/subscriber\/new?topic_id=USNLMOCPL_52\">join our mailing list<\/a>\u202fto keep up to date with\u00a0ClinVar\u00a0and other NCBI news.<\/p>\n<h5>Questions?<\/h5>\n<p>If you have questions or would like to provide feedback, please reach out to us at\u00a0<a href=\"mailto:clinvar@ncbi.nlm.nih.gov\">clinvar@ncbi.nlm.nih.gov<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>In order to support the inclusion of submitted somatic variation data, we are updating the ClinVar website. In early 2024, you will begin to see some changes. What will change? Variant (VCV) record pages will have an updated look and feel: Simpler layout with no tabs New sections will display somatic classifications Summary section will … <a href=\"https:\/\/ncbiinsights.ncbi.nlm.nih.gov\/2023\/11\/28\/updates-clinvar-website\/\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">Coming Soon! 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