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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5954861copy number variation1nstd209human GRCh38 chr20: 44,521,454-44,530,700 , GRCh37.p13 chr20: 43,150,095-43,159,341 PKIG, SERINC3
    nsv5884087copy number variation1nstd209human GRCh38 chr20: 44,521,513-44,530,655 , GRCh37.p13 chr20: 43,150,154-43,159,296 SERINC3, PKIG
    nsv5519767copy number variation1nstd206human GRCh38 chr20: 44,519,196-44,519,279 , GRCh37.p13 chr20: 43,147,837-43,147,920 SERINC3
    nsv5325566copy number variation1nstd204human GRCh38.p13 chr20: 44,248,826-44,533,449 , GRCh37.p13 chr20: 42,877,466-43,162,090 R3HDML, SERINC3, 11 more genes
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5290954copy number variation1nstd204human GRCh38.p13 chr20: 44,505,844-44,507,843 , GRCh37.p13 chr20: 43,134,485-43,136,484 SERINC3
    nsv5290254copy number variation1nstd204human GRCh38.p13 chr20: 44,248,701-44,533,500 , GRCh37.p13 chr20: 42,877,341-43,162,141 FITM2, RPL37AP1, 11 more genes
    nsv5287202copy number variation1nstd204human GRCh38.p13 chr20: 44,492,344-44,533,448 , GRCh37.p13 chr20: 43,120,985-43,162,089 SERINC3, PKIG, 1 more genes
    nsv5285846copy number variation1nstd204human GRCh38.p13 chr20: 44,473,065-44,495,243 , GRCh37.p13 chr20: 43,101,705-43,123,884 SERINC3, TTPAL
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5025638copy number variation1nstd200human GRCh38 chr20: 44,510,714-44,515,313 , GRCh37.p13 chr20: 43,139,355-43,143,954 SERINC3
    nsv5025637copy number variation1nstd200human GRCh38 chr20: 44,506,252-44,514,617 , GRCh37.p13 chr20: 43,134,893-43,143,258 SERINC3
    nsv5025631copy number variation1nstd200human GRCh38 chr20: 44,248,833-44,533,440 , GRCh37.p13 chr20: 42,877,473-43,162,081 SERINC3, HNF4A, 11 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv5012801copy number variation1nstd200human GRCh38 chr20: 44,516,656-44,519,732 , GRCh37.p13 chr20: 43,145,297-43,148,373 SERINC3
    nsv5012800copy number variation1nstd200human GRCh38 chr20: 44,515,297-44,518,818 , GRCh37.p13 chr20: 43,143,938-43,147,459 SERINC3
    nsv4884257inversion1nstd200human GRCh37 chr20: 35,583,656-44,214,103 , GRCh38.p12 chr20: 36,955,253-45,585,464 , TGM2, 180 more genes
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