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Items: 1 to 20 of 79

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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
    nsv7070383inversion1nstd229human GRCh38 chr10: 24,928,684-26,137,542 , GRCh37.p13 chr10: 25,217,613-26,426,471 RNU6-632P, HIRAP1, 13 more genes
    nsv6883337copy number variation1nstd229human GRCh38 chr10: 25,926,129-25,930,685 , GRCh37.p13 chr10: 26,215,058-26,219,614 LOC101929073
    nsv6879081copy number variation1nstd229human GRCh38 chr10: 25,788,449-25,928,663 , GRCh37.p13 chr10: 26,077,378-26,217,592 LOC101929073, RNU6-632P, 2 more genes
    nsv6589634inversion1nstd223human GRCh38 chr10: 24,928,684-26,137,542 , GRCh37.p13 chr10: 25,217,613-26,426,471 RNA5SP306, LINC00836, 13 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6240489mobile element insertion1nstd215human GRCh38 chr10: 25,927,334-25,927,334 , GRCh37.p13 chr10: 26,216,263-26,216,263 LOC101929073
    nsv6132034copy number variation1nstd213human GRCh37 chr10: 25,900,000-27,350,001 , GRCh38.p12 chr10: 25,611,071-27,061,072 GAD2, ABI1, 21 more genes
    nsv6132031copy number variation1nstd213human GRCh37 chr10: 18,100,000-28,260,001 , GRCh38.p12 chr10: 17,839,748-27,971,072 BMI1, CACNB2, 136 more genes
    nsv6002369copy number variation1nstd212human GRCh38 chr10: 25,869,052-26,740,869 , GRCh37.p13 chr10: 26,157,981-27,029,798 , SELENOOLP, 13 more genes
    nsv5309867copy number variation1nstd204human GRCh37.p13 chr10: 26,217,403-26,222,210 , GRCh38.p13 chr10: 25,928,474-25,933,281 LOC101929073, MYO3A
    nsv5250716copy number variation1nstd204human GRCh38.p13 chr10: 25,928,382-25,932,956 , GRCh37.p13 chr10: 26,217,311-26,221,885 MYO3A, LOC101929073
    nsv4975487copy number variation1nstd200human GRCh38 chr10: 25,821,361-26,080,906 , GRCh37.p13 chr10: 26,110,290-26,369,835 MYO3A, LOC101929073, 1 more genes
    nsv4560417inversion1nstd166human GRCh37.p13 chr10: 25,737,099-27,261,038 , GRCh38.p12 chr10: 25,448,170-26,972,109 , GAD2, 23 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4191606copy number variation1nstd166human GRCh37.p13 chr10: 26,217,746-26,217,899 , GRCh38.p12 chr10: 25,928,817-25,928,970 LOC101929073
    nsv4180667copy number variation1nstd166human GRCh37.p13 chr10: 26,214,393-26,220,397 , GRCh38.p12 chr10: 25,925,464-25,931,468 LOC101929073
    nsv4177400copy number variation1nstd166human GRCh37.p13 chr10: 26,067,050-26,236,921 , GRCh38.p12 chr10: 25,778,121-25,947,992 RNA5SP306, LOC101929073, 3 more genes
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