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Items: 1 to 20 of 388

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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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093856copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,262,628-104,309,873 , GRCh38.p12 chr10: 102,502,871-102,550,116 SUFU, ACTR1A
    nsv7093102copy number variation1nstd102humanLikely benign GRCh37 chr10: 104,377,195-104,377,273 , GRCh38 chr10: 102,617,438-102,617,516 SUFU
    nsv7072825inversion1nstd229human GRCh38 chr10: 102,587,595-102,594,824 , GRCh37.p13 chr10: 104,347,352-104,354,581 RNU6-43P, SUFU
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6896332copy number variation1nstd229human GRCh38 chr10: 102,606,401-102,611,000 , GRCh37.p13 chr10: 104,366,158-104,370,757 SUFU
    nsv6895309copy number variation1nstd229human GRCh38 chr10: 102,480,383-102,524,772 , GRCh37.p13 chr10: 104,240,140-104,284,529 MFSD13A, SUFU, 1 more genes
    nsv6894737copy number variation1nstd229human GRCh38 chr10: 102,536,131-102,544,536 , GRCh37.p13 chr10: 104,295,888-104,304,293 SUFU
    nsv6892901copy number variation1nstd229human GRCh38 chr10: 102,564,032-102,566,946 , GRCh37.p13 chr10: 104,323,789-104,326,703 SUFU
    nsv6892864copy number variation1nstd229human GRCh38 chr10: 102,556,656-102,557,003 , GRCh37.p13 chr10: 104,316,413-104,316,760 SUFU
    nsv6889314copy number variation1nstd229human GRCh38 chr10: 102,567,187-102,572,533 , GRCh37.p13 chr10: 104,326,944-104,332,290 RPL23AP58, SUFU
    nsv6887091copy number variation1nstd229human GRCh38 chr10: 102,527,384-102,534,915 , GRCh37.p13 chr10: 104,287,141-104,294,672 SUFU
    nsv6885521copy number variation1nstd229human GRCh38 chr10: 102,611,465-102,611,618 , GRCh37.p13 chr10: 104,371,222-104,371,375 SUFU
    nsv6881193copy number variation1nstd229human GRCh38 chr10: 102,585,387-102,585,885 , GRCh37.p13 chr10: 104,345,144-104,345,642 SUFU
    nsv6880024copy number variation1nstd229human GRCh38 chr10: 102,603,615-102,603,650 , GRCh37.p13 chr10: 104,363,372-104,363,407 SUFU
    nsv6878777copy number variation1nstd229human GRCh38 chr10: 102,527,301-102,536,600 , GRCh37.p13 chr10: 104,287,058-104,296,357 SUFU
    nsv6637556copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,031,306-104,366,150 , GRCh38.p12 chr10: 102,271,549-102,606,393 CUEDC2, C10orf95, 12 more genes
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