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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5273531copy number variation1nstd204human GRCh38.p13 chr15: 33,908,501-34,437,400 , GRCh37.p13 chr15: 34,200,702-34,729,601 , GOLGA8A, 14 more genes
    nsv5158016mobile element insertion1nstd203human GRCh38 chr15: 34,361,123-34,361,138 , GRCh37.p13 chr15: 34,653,324-34,653,339 LPCAT4
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4749247copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,700,525 , GRCh38.p12 chr15: 28,914,297-34,408,324 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , HNRNPA1P71, 132 more genes
    nsv4742703copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,846,747 , GRCh38.p12 chr15: 28,914,297-34,554,546 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , KATNBL1, 138 more genes
    nsv4729489copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,914,238-34,879,217 , GRCh38.p12 chr15: 32,622,037-34,587,016 RYR3, ARHGAP11A, 35 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
    nsv4674936copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278 SNORD115-48, MIR4509-2, 330 more genes
    nsv4620138copy number variation1nstd183human GRCh37 chr15: 32,770,109-34,830,944 , GRCh38.p12 chr15: 32,477,908-34,538,743 , GRCh38.p12 chr15|NT_187660.1: 2,721,395-5,161,414 , LINC03034, 88 more genes
    nsv4529143copy number variation1nstd166human GRCh37.p13 chr15: 34,459,999-34,679,000 , GRCh38.p12 chr15: 34,167,798-34,386,799 SLC12A6, GOLGA8A, 7 more genes
    nsv4499256mobile element insertion1nstd166human GRCh37.p13 chr15: 34,653,324-34,653,324 , GRCh38.p12 chr15: 34,361,123-34,361,123 LPCAT4
    nsv4457308copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,915,592-34,671,601 , GRCh38.p12 chr15: 32,623,391-34,379,400 LPCAT4, PGBD4, 27 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4430872copy number variation1nstd174human GRCh37 chr15: 34,657,736-34,700,792 , GRCh38.p12 chr15: 34,365,535-34,408,591 ACTG1P15, LOC100422491, 3 more genes
    nsv4425673copy number variation1nstd174human GRCh37 chr15: 32,896,350-35,372,508 , GRCh38.p12 chr15: 32,604,149-35,080,307 , ACTC1, 50 more genes
    nsv4420833copy number variation1nstd174human GRCh37 chr15: 34,658,419-34,877,753 , GRCh38.p12 chr15: 34,366,218-34,585,552 GOLGA8A, LOC100422491, 9 more genes
    nsv3967951copy number variation1nstd168human GRCh38 chr15: 34,359,930-34,534,184 , GRCh37.p13 chr15: 34,652,131-34,826,385 GOLGA8A, FSCN1P1, 8 more genes
    nsv3966156insertion1nstd168human GRCh38 chr15: 34,314,421-34,387,963 , GRCh37.p13 chr15: 34,606,622-34,680,164 SLC12A6, GOLGA8A, 5 more genes
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