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Items: 1 to 20 of 87

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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
    nsv7093877copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,227,463-53,769,653 , GRCh38.p12 chr10: 51,467,703-52,009,893 PRKG1, CSTF2T
    nsv7076978inversion1nstd229human GRCh38 chr10: 49,556,263-52,217,922 , GRCh37.p13 chr10: 50,764,309-53,977,682 A1CF, NPAP1P1, 36 more genes
    nsv7060309inversion1nstd229human GRCh38 chr10: 46,173,677-55,799,586 , GRCh37.p13 chr10: 46,591,857-57,559,346 NPY4R, LOC102724603, 138 more genes
    nsv6892329copy number variation1nstd229human GRCh38 chr10: 51,537,991-52,321,754 , GRCh37.p13 chr10: 53,297,751-54,081,514 PRKG1, PRKG1-AS1, 2 more genes
    nsv6885623copy number variation1nstd229human GRCh38 chr10: 51,671,754-51,781,751 , GRCh37.p13 chr10: 53,431,514-53,541,511 CSTF2T, PRKG1
    nsv6884408copy number variation1nstd229human GRCh38 chr10: 51,622,887-51,789,984 , GRCh37.p13 chr10: 53,382,647-53,549,744 CSTF2T, PRKG1
    nsv6879085copy number variation1nstd229human GRCh38 chr10: 51,375,001-52,053,000 , GRCh37.p13 chr10: 53,134,761-53,812,760 PRKG1, CSTF2T
    nsv6441234copy number variation1nstd223human GRCh38 chr10: 51,537,991-52,321,749 , GRCh37.p13 chr10: 53,297,751-54,081,509 CSTF2T, DKK1, 2 more genes
    nsv6314082copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,134,455-53,811,118 , GRCh38.p12 chr10: 51,374,695-52,051,358 PRKG1, CSTF2T
    nsv6132043copy number variation1nstd213human GRCh37 chr10: 53,050,000-53,540,001 , GRCh38.p12 chr10: 51,290,240-51,780,241 PRKG1, CSTF2T, 2 more genes
    nsv5477543copy number variation1nstd206human GRCh38 chr10: 51,699,583-51,699,665 , GRCh37.p13 chr10: 53,459,343-53,459,425 PRKG1, CSTF2T
    nsv5319080copy number variation1nstd204human GRCh37.p13 chr10: 53,189,906-54,198,554 , GRCh38.p13 chr10: 51,430,146-52,438,794 PRKG1, DKK1, 4 more genes
    nsv5318262copy number variation1nstd204human GRCh37.p13 chr10: 53,456,149-53,456,555 , GRCh38.p13 chr10: 51,696,389-51,696,795 CSTF2T, PRKG1
    nsv5254843copy number variation1nstd204human GRCh38.p13 chr10: 51,665,782-51,717,999 , GRCh37.p13 chr10: 53,425,542-53,477,759 PRKG1, CSTF2T
    nsv5251820copy number variation1nstd204human GRCh38.p13 chr10: 51,429,901-51,712,600 , GRCh37.p13 chr10: 53,189,661-53,472,360 CSTF2T, PRKG1
    nsv5246779copy number variation1nstd204human GRCh38.p13 chr10: 51,692,227-51,717,774 , GRCh37.p13 chr10: 53,451,987-53,477,534 CSTF2T, PRKG1
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973632copy number variation1nstd200human GRCh38 chr10: 51,639,980-51,699,074 , GRCh37.p13 chr10: 53,399,740-53,458,834 PRKG1, CSTF2T
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