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Items: 1 to 20 of 1401

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125474copy number variation1nstd186human GRCh37 chr22: 22,840,665-22,840,756 , GRCh38.p12 chr22|NT_187629.1: 121,980-122,071 , GRCh38.p12 chr22: 22,486,323-22,486,414 IGL, ZNF280B
    nsv5392014copy number variation3nstd186human GRCh37 chr22: 22,906,059-22,909,454 , GRCh38.p12 chr22|NT_187629.1: 199,311-202,706 , GRCh38.p12 chr22: 22,563,654-22,567,049 LL22NC03-63E9.3, IGL
    nsv5391717copy number variation3nstd186human GRCh37 chr22: 22,922,732-22,928,712 , GRCh38.p12 chr22: 22,580,268-22,586,241 , GRCh38.p12 chr22|NT_187629.1: 215,925-221,898 IGL, IGLV2-34, 1 more genes
    nsv5389594copy number variation1nstd186human GRCh37 chr22: 22,928,305-22,928,441 , GRCh38.p12 chr22: 22,585,841-22,585,970 , GRCh38.p12 chr22|NT_187629.1: 221,498-221,627 IGL
    nsv5333601translocation1nstd200human GRCh37 chr22: 22,717,200-22,717,200 , GRCh37 chr22: 22,743,406-22,743,406 , GRCh38.p12 chr22: 22,362,840-22,362,840 , GRCh38.p12 chr22|NT_187629.1: 15,591-15,591 , GRCh38.p12 chr22: 22,389,038-22,389,038 IGL
    nsv4869362copy number variation1nstd200human GRCh37 chr22: 22,870,654-22,873,890 , GRCh38.p12 chr22: 22,516,318-22,519,547 , GRCh38.p12 chr22|NT_187629.1: 151,975-155,204 IGL, ZNF280A, 1 more genes
    nsv4869361copy number variation1nstd200human GRCh37 chr22: 22,849,196-22,853,465 , GRCh38.p12 chr22: 22,494,877-22,499,155 , GRCh38.p12 chr22|NT_187629.1: 130,534-134,812 ZNF280B, IGL
    nsv4869360copy number variation1nstd200human GRCh37 chr22: 22,820,719-22,820,941 , GRCh38.p12 chr22: 22,466,382-22,466,604 , GRCh38.p12 chr22|NT_187629.1: 102,022-102,244 IGL
    nsv4869359copy number variation1nstd200human GRCh37 chr22: 22,753,308-22,776,758 , GRCh38.p12 chr22: 22,398,973-22,422,421 , GRCh38.p12 chr22|NT_187629.1: 34,623-58,059 IGLV1-40, ASH2LP1, 7 more genes
    nsv4869131copy number variation1nstd200human GRCh37 chr22: 22,953,734-22,955,429 , GRCh38.p12 chr22: 22,611,264-22,612,959 , GRCh38.p12 chr22|NT_187629.1: 246,921-248,616 IGL
    nsv4869130copy number variation1nstd200human GRCh37 chr22: 22,922,732-22,928,712 , GRCh38.p12 chr22: 22,580,268-22,586,241 , GRCh38.p12 chr22|NT_187629.1: 215,925-221,898 IGLV2-33, IGLV2-34, 1 more genes
    nsv4869129copy number variation1nstd200human GRCh37 chr22: 22,906,059-22,909,454 , GRCh38.p12 chr22: 22,563,654-22,567,049 , GRCh38.p12 chr22|NT_187629.1: 199,311-202,706 LL22NC03-63E9.3, IGL
    nsv4869128copy number variation1nstd200human GRCh37 chr22: 22,886,394-22,887,697 , GRCh38.p12 chr22|NT_187629.1: 179,626-180,930 , GRCh38.p12 chr22: 22,543,969-22,545,273 LOC105379601, IGL
    nsv4869127copy number variation1nstd200human GRCh37 chr22: 22,797,577-22,800,570 , GRCh38.p12 chr22: 22,443,240-22,446,232 , GRCh38.p12 chr22|NT_187629.1: 78,878-81,871 IGL, LOC100736412
    nsv4869126copy number variation1nstd200human GRCh37 chr22: 22,791,139-22,792,881 , GRCh38.p12 chr22|NT_187629.1: 72,440-74,182 , GRCh38.p12 chr22: 22,436,802-22,438,544 IGL
    nsv4869121copy number variation1nstd200human GRCh37 chr22: 22,724,448-23,235,964 , GRCh38.p12 chr22: 22,370,080-22,893,784 , GRCh38.p12 chr22|NT_187629.1: 1-259,914 , IGLVI-20, 78 more genes
    nsv4758935insertion1nstd199human GRCh37 chr22: 22,926,228-22,926,228 , GRCh38.p12 chr22: 22,583,764-22,583,764 , GRCh38.p12 chr22|NT_187629.1: 219,421-219,421 IGL
    nsv4751424insertion1nstd199human GRCh37 chr22: 22,703,502-22,703,502 , GRCh38.p12 chr22: 22,349,152-22,349,152 , GRCh38.p12 chr22|NT_187629.1: 25,343-25,343 IGL
    nsv4747819copy number variation1nstd199human GRCh37 chr22: 22,796,261-22,796,312 , GRCh38.p12 chr22|NT_187629.1: 77,562-77,613 , GRCh38.p12 chr22: 22,441,924-22,441,975 IGL
    nsv4741239copy number variation1nstd199human GRCh37 chr22: 22,920,891-22,920,942 , GRCh38.p12 chr22: 22,578,451-22,578,502 , GRCh38.p12 chr22|NT_187629.1: 214,108-214,159 IGL, IGLV2-34
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