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Items: 1 to 20 of 210

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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
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7076085inversion1nstd229human GRCh38 chr10: 94,697,612-94,958,568 , GRCh37.p13 chr10: 96,457,369-96,718,325 CYP2C19, MTND4P20, 6 more genes
    nsv7060443inversion1nstd229human GRCh38 chr10: 94,671,513-95,794,260 , GRCh37.p13 chr10: 96,431,270-97,554,017 ENTPD1, RPL7AP52, 20 more genes
    nsv6896107copy number variation1nstd229human GRCh38 chr10: 94,375,560-95,464,831 , GRCh37.p13 chr10: 96,135,317-97,224,588 SORBS1, MTND4P19, 18 more genes
    nsv6894874copy number variation1nstd229human GRCh38 chr10: 94,865,302-95,004,477 , GRCh37.p13 chr10: 96,625,059-96,764,234 RPL7AP52, CYP2C115P, 4 more genes
    nsv6894841copy number variation1nstd229human GRCh38 chr10: 94,882,668-95,007,072 , GRCh37.p13 chr10: 96,642,425-96,766,829 CYP2C9, RPL7AP52, 4 more genes
    nsv6894172copy number variation1nstd229human GRCh38 chr10: 94,990,101-95,010,300 , GRCh37.p13 chr10: 96,749,858-96,770,057 CYP2C59P, LOC107984256, 2 more genes
    nsv6893520copy number variation1nstd229human GRCh38 chr10: 94,879,137-95,091,511 , GRCh37.p13 chr10: 96,638,894-96,851,268 CYP2C115P, LOC107984256, 6 more genes
    nsv6891231copy number variation1nstd229human GRCh38 chr10: 94,932,951-94,942,820 , GRCh37.p13 chr10: 96,692,708-96,702,577 MTND4P20, CYP2C9
    nsv6881218copy number variation1nstd229human GRCh38 chr10: 94,954,059-94,954,110 , GRCh37.p13 chr10: 96,713,816-96,713,867 CYP2C9
    nsv6879979copy number variation1nstd229human GRCh38 chr10: 94,785,301-94,940,600 , GRCh37.p13 chr10: 96,545,058-96,700,357 CYP2C19, MTND4P20, 4 more genes
    nsv6878596copy number variation1nstd229human GRCh38 chr10: 94,956,489-95,106,905 , GRCh37.p13 chr10: 96,716,246-96,866,662 LOC107984256, CYP2C8, 3 more genes
    nsv6637999copy number variation1nstd102humanUncertain significance GRCh37 chr10: 96,155,285-97,224,160 , GRCh38.p12 chr10: 94,395,528-95,464,403 CYP2C58P, CTBP2P2, 18 more genes
    nsv6620937copy number variation1nstd224human GRCh37 chr10: 96,612,596-96,744,732 , GRCh38.p12 chr10: 94,852,839-94,984,975 CYP2C19, CYP2C9, 4 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6451140copy number variation1nstd223human GRCh38 chr10: 94,942,601-94,945,000 , GRCh37.p13 chr10: 96,702,358-96,704,757 CYP2C9
    nsv6447258copy number variation1nstd223human GRCh38 chr10: 94,975,701-94,976,600 , GRCh37.p13 chr10: 96,735,458-96,736,357 CYP2C9
    nsv6444755copy number variation1nstd223human GRCh38 chr10: 94,961,801-94,963,100 , GRCh37.p13 chr10: 96,721,558-96,722,857 CYP2C9
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