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Items: 1 to 20 of 370

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7075417inversion1nstd229human GRCh38 chr10: 105,415,390-106,017,073 , GRCh37.p13 chr10: 107,175,148-107,776,831 YWHAZP5, LOC105378468, 4 more genes
    nsv7062616inversion1nstd229human GRCh38 chr10: 105,706,269-105,711,432 , GRCh37.p13 chr10: 107,466,027-107,471,190 LINC02627
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7061057inversion1nstd229human GRCh38 chr10: 105,711,192-105,715,830 , GRCh37.p13 chr10: 107,470,950-107,475,588 LINC02627
    nsv6896307copy number variation1nstd229human GRCh38 chr10: 105,668,870-105,710,308 , GRCh37.p13 chr10: 107,428,628-107,470,066 LOC107984266, LINC02627, 1 more genes
    nsv6895031copy number variation1nstd229human GRCh38 chr10: 105,808,053-105,892,711 , GRCh37.p13 chr10: 107,567,811-107,652,469 LINC02627
    nsv6894390copy number variation1nstd229human GRCh38 chr10: 105,684,978-105,690,385 , GRCh37.p13 chr10: 107,444,736-107,450,143 LINC02627, YWHAZP5
    nsv6892170copy number variation1nstd229human GRCh38 chr10: 105,806,399-105,808,688 , GRCh37.p13 chr10: 107,566,157-107,568,446 LINC02627
    nsv6891685copy number variation1nstd229human GRCh38 chr10: 104,811,653-105,834,977 , GRCh37.p13 chr10: 106,571,411-107,594,735 LOC107984266, YWHAZP5, 6 more genes
    nsv6890947copy number variation1nstd229human GRCh38 chr10: 105,748,767-105,755,514 , GRCh37.p13 chr10: 107,508,525-107,515,272 LINC02627
    nsv6889897copy number variation1nstd229human GRCh38 chr10: 104,960,985-105,815,666 , GRCh37.p13 chr10: 106,720,743-107,575,424 LOC107984266, LINC02627, 6 more genes
    nsv6888763copy number variation1nstd229human GRCh38 chr10: 105,751,508-105,752,705 , GRCh37.p13 chr10: 107,511,266-107,512,463 LINC02627
    nsv6887401copy number variation1nstd229human GRCh38 chr10: 105,649,778-105,706,549 , GRCh37.p13 chr10: 107,409,536-107,466,307 LOC107984266, LINC02627, 1 more genes
    nsv6886291copy number variation1nstd229human GRCh38 chr10: 105,802,107-105,810,244 , GRCh37.p13 chr10: 107,561,865-107,570,002 LINC02627
    nsv6885991copy number variation1nstd229human GRCh38 chr10: 105,681,500-105,692,125 , GRCh37.p13 chr10: 107,441,258-107,451,883 LINC02627, YWHAZP5
    nsv6882633copy number variation1nstd229human GRCh38 chr10: 105,687,872-105,707,983 , GRCh37.p13 chr10: 107,447,630-107,467,741 YWHAZP5, LINC02627
    nsv6881360copy number variation1nstd229human GRCh38 chr10: 105,755,810-105,771,519 , GRCh37.p13 chr10: 107,515,568-107,531,277 LINC02627
    nsv6880944copy number variation1nstd229human GRCh38 chr10: 105,687,616-105,687,666 , GRCh37.p13 chr10: 107,447,374-107,447,424 LINC02627, YWHAZP5
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