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Items: 1 to 20 of 230

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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
    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
    nsv7094310copy number variation1nstd102humanUncertain significance GRCh37 chr15: 85,186,701-85,197,505 , GRCh38.p12 chr15: 84,643,470-84,654,274 WDR73, NMB
    nsv7072278inversion1nstd229human GRCh38 chr15: 84,569,692-85,414,726 , GRCh37.p13 chr15: 85,112,923-85,957,957 ZNF592, UBE2Q2P1, 27 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
    nsv7066342inversion1nstd229human GRCh38 chr15: 84,626,965-85,448,342 , GRCh37.p13 chr15: 85,170,196-85,991,573 WDR73, AKAP13, 23 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
    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
    nsv6970972copy number variation1nstd229human GRCh38 chr15: 84,646,794-84,934,217 , GRCh37.p13 chr15: 85,190,025-85,477,448 ZNF592, ALPK3, 4 more genes
    nsv6970608copy number variation1nstd229human GRCh38 chr15: 84,568,332-84,711,758 , GRCh37.p13 chr15: 85,111,563-85,254,989 SEC11A, SCAND2P, 7 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
    nsv6965548copy number variation1nstd229human GRCh38 chr15: 84,646,659-84,646,826 , GRCh37.p13 chr15: 85,189,890-85,190,057 WDR73
    nsv6963468copy number variation1nstd229human GRCh38 chr15: 84,607,501-84,665,100 , GRCh37.p13 chr15: 85,150,732-85,208,331 WDR73, NMB, 4 more genes
    nsv6962770copy number variation1nstd229human GRCh38 chr15: 84,639,069-84,639,634 , GRCh37.p13 chr15: 85,182,300-85,182,865 WDR73, SCAND2P
    nsv6960945copy number variation1nstd229human GRCh38 chr15: 84,641,053-84,641,241 , GRCh37.p13 chr15: 85,184,284-85,184,472 WDR73, SCAND2P
    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
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