U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

Search results

Items: 2

1.

rs207482233 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TCATACAGGTCATCGCT>GC [Show Flanks]
    Chromosome:
    4:186201149 (GRCh38)
    4:187122303 (GRCh37)
    Canonical SPDI:
    NC_000004.12:186201148:TCATACAGGTCATCGCT:GC
    Gene:
    CYP4V2 (Varview)
    Functional Consequence:
    coding_sequence_variant,splice_acceptor_variant,intron_variant
    Clinical significance:
    pathogenic
    Validated:
    by cluster
    HGVS:

    2.

    rs527236049 has merged into rs207482233 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TCATACAGGTCATCGCT>GC [Show Flanks]
      Chromosome:
      4:186201149 (GRCh38)
      4:187122303 (GRCh37)
      Canonical SPDI:
      NC_000004.12:186201148:TCATACAGGTCATCGCT:GC
      Gene:
      CYP4V2 (Varview)
      Functional Consequence:
      coding_sequence_variant,splice_acceptor_variant,intron_variant
      Clinical significance:
      pathogenic
      Validated:
      by cluster
      HGVS:

      Supplemental Content

      Filters: Manage Filters

      Find related data

      Search details

      See more...

      Recent activity

      Clear Turn Off Turn On

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...