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Items: 1 to 20 of 526

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146627copy number variation1nstd232human GRCh37.p13 chr10: 15,271,739-15,271,885 , GRCh38.p12 chr10: 15,229,740-15,229,886 FAM171A1
    nsv7140426insertion1nstd232human GRCh37.p13 chr10: 15,379,583-15,379,583 , GRCh38.p12 chr10: 15,337,584-15,337,584 FAM171A1
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7070703inversion1nstd229human GRCh38 chr10: 15,321,812-15,324,594 , GRCh37.p13 chr10: 15,363,811-15,366,593 FAM171A1
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv6896494copy number variation1nstd229human GRCh38 chr10: 15,007,737-15,362,330 , GRCh37.p13 chr10: 15,049,736-15,404,329 RPP38, ACBD7, 14 more genes
    nsv6895187copy number variation1nstd229human GRCh38 chr10: 15,290,601-15,297,500 , GRCh37.p13 chr10: 15,332,600-15,339,499 FAM171A1
    nsv6894457copy number variation1nstd229human GRCh38 chr10: 15,305,355-15,307,716 , GRCh37.p13 chr10: 15,347,354-15,349,715 FAM171A1
    nsv6894337copy number variation1nstd229human GRCh38 chr10: 15,256,098-15,256,297 , GRCh37.p13 chr10: 15,298,097-15,298,296 FAM171A1
    nsv6893991copy number variation1nstd229human GRCh38 chr10: 15,292,280-15,297,383 , GRCh37.p13 chr10: 15,334,279-15,339,382 FAM171A1
    nsv6893267copy number variation1nstd229human GRCh38 chr10: 15,323,610-15,356,424 , GRCh37.p13 chr10: 15,365,609-15,398,423 FAM171A1
    nsv6890999copy number variation1nstd229human GRCh38 chr10: 15,284,609-15,308,862 , GRCh37.p13 chr10: 15,326,608-15,350,861 FAM171A1
    nsv6889515copy number variation1nstd229human GRCh38 chr10: 15,263,860-15,263,956 , GRCh37.p13 chr10: 15,305,859-15,305,955 FAM171A1
    nsv6889141copy number variation1nstd229human GRCh38 chr10: 15,317,823-15,323,594 , GRCh37.p13 chr10: 15,359,822-15,365,593 FAM171A1
    nsv6887942copy number variation1nstd229human GRCh38 chr10: 15,236,606-15,239,769 , GRCh37.p13 chr10: 15,278,605-15,281,768 FAM171A1, LOC105376433
    nsv6887098copy number variation1nstd229human GRCh38 chr10: 15,216,102-15,532,821 , GRCh37.p13 chr10: 15,258,101-15,574,820 LOC105376433, ITGA8, 1 more genes
    nsv6885685copy number variation1nstd229human GRCh38 chr10: 15,225,101-15,228,800 , GRCh37.p13 chr10: 15,267,100-15,270,799 FAM171A1
    nsv6885052copy number variation1nstd229human GRCh38 chr10: 15,301,613-15,312,977 , GRCh37.p13 chr10: 15,343,612-15,354,976 FAM171A1
    nsv6883677copy number variation1nstd229human GRCh38 chr10: 15,365,401-15,383,900 , GRCh37.p13 chr10: 15,407,400-15,425,899 FAM171A1
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