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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7143888copy number variation1nstd232human GRCh37.p13 chr15: 85,055,739-85,055,801 , GRCh38.p12 chr15: 84,512,508-84,512,570 GOLGA6L5P
    nsv7137120copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,908,070-85,681,134 , GRCh38.p12 chr15: 84,239,318-85,137,903 UBE2Q2P1, ZSCAN2, 32 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7074802inversion1nstd229human GRCh38 chr15: 84,391,455-84,541,392 , GRCh37.p13 chr15: 84,946,153-85,084,623 LOC102724135, RN7SL417P, 13 more genes
    nsv7068416inversion1nstd229human GRCh38 chr15: 84,126,042-85,592,094 , GRCh37.p13 chr15: 82,808,513-86,135,325 DNM1P44, RN7SL417P, 53 more genes
    nsv7067903inversion1nstd229human GRCh38 chr15: 82,416,076-84,530,844 , GRCh37.p13 chr15: 82,708,281-85,074,075 RN7SL417P, FABP5P8, 66 more genes
    nsv7067626inversion1nstd229human GRCh38 chr15: 83,773,391-84,546,163 , GRCh37.p13 chr15: 82,808,513-85,089,394 LOC105376722, RNU6-1339P, 29 more genes
    nsv7065371inversion1nstd229human GRCh38 chr15: 82,262,265-85,274,261 , GRCh37.p13 chr15: 82,554,606-85,817,492 GOLGA6L10, GOLGA6L17P, 96 more genes
    nsv7059644inversion1nstd229human GRCh38 chr15: 82,398,536-84,548,330 , GRCh37.p13 chr15: 82,690,748-85,091,561 LOC102724093, CSPG4P11, 66 more genes
    nsv7059555inversion1nstd229human GRCh38 chr15: 84,402,911-85,382,177 , GRCh37.p13 chr15: 84,957,609-85,925,408 UBE2Q2P11, SCAND2P, 36 more genes
    nsv7058879inversion1nstd229human GRCh38 chr15: 82,197,935-85,119,504 , GRCh37.p13 chr15: 82,490,276-85,662,735 LOC103171574, RN7SL417P, 87 more genes
    nsv6966079copy number variation1nstd229human GRCh38 chr15: 83,082,381-85,945,931 , GRCh37.p13 chr15: 82,808,513-86,489,162 LOC105370936, LOC105370933, 74 more genes
    nsv6637907copy number variation1nstd102humanUncertain significance GRCh37 chr15: 84,910,816-85,786,847 , GRCh38.p12 chr15: 84,242,064-85,243,616 LOC102724117, ZNF592, 39 more genes
    nsv6637904copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 84,827,469-85,786,847 , GRCh38.p12 chr15: 84,158,717-85,243,616 NMB, PDE8A, 46 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6593088inversion1nstd223human GRCh38 chr15: 84,391,454-84,541,391 , GRCh37.p13 chr15: 84,946,152-85,084,622 LOC102724135, DNM1P44, 13 more genes
    nsv6578911inversion1nstd223human GRCh38 chr15: 77,618,608-84,708,062 , GRCh37.p13 chr15: 77,910,950-85,251,293 TMC3-AS1, LOC642677, 177 more genes
    nsv6306327copy number variation1nstd186human GRCh37 chr15: 85,051,297-85,058,914 , GRCh38.p12 chr15: 84,508,066-84,515,683 GOLGA6L5P
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