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Items: 1 to 20 of 222

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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
    nsv7071026inversion1nstd229human GRCh38 chr10: 97,392,346-97,397,347 , GRCh37.p13 chr10: 99,152,103-99,157,104 RPL34P20, RRP12
    nsv7062571inversion1nstd229human GRCh38 chr10: 97,388,596-97,388,696 , GRCh37.p13 chr10: 99,148,353-99,148,453 RRP12
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897085copy number variation1nstd229human GRCh38 chr10: 97,386,839-97,394,994 , GRCh37.p13 chr10: 99,146,596-99,154,751 RRP12, RPL34P20
    nsv6894405copy number variation1nstd229human GRCh38 chr10: 97,376,467-97,379,140 , GRCh37.p13 chr10: 99,136,224-99,138,897 RRP12
    nsv6886722copy number variation1nstd229human GRCh38 chr10: 97,320,001-97,390,200 , GRCh37.p13 chr10: 99,079,758-99,149,957 RRP12, LOC105378448, 2 more genes
    nsv6886089copy number variation1nstd229human GRCh38 chr10: 97,352,518-97,357,247 , GRCh37.p13 chr10: 99,112,275-99,117,004 RRP12
    nsv6885955copy number variation1nstd229human GRCh38 chr10: 97,182,219-97,365,920 , GRCh37.p13 chr10: 98,941,976-99,125,677 RRP12, LOC105378447, 8 more genes
    nsv6883101copy number variation1nstd229human GRCh38 chr10: 97,369,449-97,375,310 , GRCh37.p13 chr10: 99,129,206-99,135,067 RRP12
    nsv6882546copy number variation1nstd229human GRCh38 chr10: 97,363,461-97,363,478 , GRCh37.p13 chr10: 99,123,218-99,123,235 RRP12
    nsv6881411copy number variation1nstd229human GRCh38 chr10: 97,282,801-97,378,900 , GRCh37.p13 chr10: 99,042,558-99,138,657 RRP12, ARHGAP19, 5 more genes
    nsv6880683copy number variation1nstd229human GRCh38 chr10: 97,334,301-97,865,700 , GRCh37.p13 chr10: 99,094,058-99,625,457 FRAT2, LOC105378448, 21 more genes
    nsv6880682copy number variation1nstd229human GRCh38 chr10: 97,224,366-98,323,209 , GRCh37.p13 chr10: 98,984,123-100,082,966 ZDHHC16, RPL34P20, 29 more genes
    nsv6880393copy number variation1nstd229human GRCh38 chr10: 97,245,070-97,586,825 , GRCh37.p13 chr10: 99,004,827-99,346,582 LOC644215, ARHGAP19, 14 more genes
    nsv6637978copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,027,360-99,300,723 , GRCh38.p12 chr10: 97,267,603-97,540,966 RPL12P27, ARHGAP19-SLIT1, 12 more genes
    nsv6620786copy number variation1nstd224human GRCh37 chr10: 98,942,021-99,116,903 , GRCh38.p12 chr10: 97,182,264-97,357,146 RPL12P27, FRAT2, 8 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6576804inversion1nstd223human GRCh38 chr10: 97,391,452-97,392,268 , GRCh37.p13 chr10: 99,151,209-99,152,025 RRP12, RPL34P20
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