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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6506104copy number variation1nstd223human GRCh38 chr15: 34,976,999-34,977,286 , GRCh37.p13 chr15: 35,269,200-35,269,487 ZNF770
    nsv6498543copy number variation1nstd223human GRCh38 chr15: 34,988,101-34,988,500 , GRCh37.p13 chr15: 35,280,302-35,280,701 LOC105370764, ZNF770
    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
    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
    nsv6083647insertion1nstd212human GRCh38 chr15: 34,979,916-34,979,916 , GRCh37.p13 chr15: 35,272,117-35,272,117 ZNF770
    nsv5709574mobile element insertion1nstd211human GRCh38 chr15: 34,979,935-34,979,935 , GRCh37.p13 chr15: 35,272,136-35,272,136 ZNF770
    nsv5505915copy number variation1nstd206human GRCh38 chr15: 34,940,957-34,978,469 , GRCh37.p13 chr15: 35,233,158-35,270,670 AQR, RPL36AP8, 1 more genes
    nsv5423353mobile element insertion1nstd206human GRCh38 chr15: 34,979,935-34,979,986 , GRCh37.p13 chr15: 35,272,136-35,272,187 ZNF770
    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
    nsv5198826mobile element insertion1nstd203human GRCh38 chr15: 34,977,413-34,977,428 , GRCh37.p13 chr15: 35,269,614-35,269,629 ZNF770
    nsv5001220copy number variation1nstd200human GRCh38 chr15: 34,976,994-34,977,286 , GRCh37.p13 chr15: 35,269,195-35,269,487 ZNF770
    nsv4855831copy number variation1nstd200human GRCh37 chr15: 35,269,195-35,269,487 , GRCh38.p12 chr15: 34,976,994-34,977,286 ZNF770
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 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
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