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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094366copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,526,072-35,087,019 , GRCh38.p12 chr15: 34,233,871-34,794,818 NUTM1, ACTC1, 16 more genes
    nsv7071130inversion1nstd229human GRCh38 chr15: 33,339,608-35,270,089 , GRCh37.p13 chr15: 33,631,809-35,562,290 LOC105370765, AQR, 38 more genes
    nsv7063469inversion1nstd229human GRCh38 chr15: 33,686,568-35,388,285 , GRCh37.p13 chr15: 33,978,769-35,680,486 NUTM1, AVEN, 41 more genes
    nsv6977406copy number variation1nstd229human GRCh38 chr15: 34,649,497-35,222,830 , GRCh37.p13 chr15: 34,941,698-35,515,031 LOC105370764, PRELID1P4, 14 more genes
    nsv6977169copy number variation1nstd229human GRCh38 chr15: 34,785,976-34,839,814 , GRCh37.p13 chr15: 35,078,177-35,132,015 LOC107984776, ACTC1, 1 more genes
    nsv6974648copy number variation1nstd229human GRCh38 chr15: 34,685,969-35,270,610 , GRCh37.p13 chr15: 34,978,170-35,562,811 ANP32AP1, LOC107984776, 14 more genes
    nsv6963494copy number variation1nstd229human GRCh38 chr15: 34,690,573-35,049,113 , GRCh37.p13 chr15: 34,982,774-35,341,314 LOC107984776, TUBAP11, 8 more genes
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6314628insertion1nstd102humanUncertain significance GRCh38 chr15: 34,791,099-34,791,099 , GRCh37 chr15: 35,083,300-35,083,300 ACTC1, GJD2-DT
    nsv6309784copy number variation1nstd102humanUncertain significance GRCh37 chr15: 34,526,082-35,087,009 , GRCh38.p12 chr15: 34,233,881-34,794,808 NUTM1, DNM1P5, 16 more genes
    nsv6132893copy number variation1nstd213human GRCh37 chr15: 34,900,000-36,170,001 , GRCh38.p12 chr15: 34,607,799-35,877,800 ANP32AP1, HNRNPA1P45, 20 more genes
    nsv6132892copy number variation1nstd213human GRCh37 chr15: 34,710,000-35,360,001 , GRCh38.p12 chr15: 34,417,799-35,067,800 LOC105370763, ACTC1, 16 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5005262copy number variation1nstd200human GRCh38 chr15: 34,746,264-34,886,834 , GRCh37.p13 chr15: 35,038,465-35,179,035 ACTC1, AQR, 4 more genes
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4682802copy number variation2nstd102humanUncertain significance GRCh37 chr15: 35,080,829-35,087,019 , GRCh38.p12 chr15: 34,788,628-34,794,818 GJD2-DT, ACTC1
    nsv4680465copy number variation1nstd189human GRCh37.p13 chr15: 34,771,762-35,203,705 , GRCh38.p12 chr15: 34,479,561-34,911,504 ACTC1, AQR, 11 more genes
    nsv4679586copy number variation1nstd189human GRCh37.p13 chr15: 35,059,342-35,171,068 , GRCh38.p12 chr15: 34,767,141-34,878,867 ACTC1, AQR, 3 more genes
    nsv4675702copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,675,452-35,689,958 , GRCh38.p12 chr15: 31,383,249-35,397,757 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 AVEN, PRELID1P4, 113 more genes
    nsv4675391copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053 TPST2P1, AVEN, 65 more genes
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