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Items: 1 to 20 of 392

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933954copy number variation1nstd209human GRCh38 chr14: 99,185,473-99,185,777 , GRCh37.p13 chr14: 99,651,810-99,652,114 BCL11B
    nsv5863314copy number variation2nstd209human GRCh38 chr14: 99,255,627-99,257,026 , GRCh37.p13 chr14: 99,721,964-99,723,363 BCL11B
    nsv5591621copy number variation1nstd207human GRCh38 chr14: 99,199,670-99,199,727 , GRCh37.p13 chr14: 99,666,007-99,666,064 BCL11B
    nsv5512172copy number variation1nstd206human GRCh38 chr14: 99,168,884-99,169,004 , GRCh37.p13 chr14: 99,635,221-99,635,341 BCL11B
    nsv5508100copy number variation1nstd206human GRCh38 chr14: 99,185,467-99,185,778 , GRCh37.p13 chr14: 99,651,804-99,652,115 BCL11B
    nsv5503879copy number variation1nstd206human GRCh38 chr14: 99,268,595-99,268,664 , GRCh37.p13 chr14: 99,734,932-99,735,001 BCL11B
    nsv5502777copy number variation1nstd206human GRCh38 chr14: 99,208,959-99,209,024 , GRCh37.p13 chr14: 99,675,296-99,675,361 BCL11B
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5314863copy number variation1nstd204human GRCh38.p13 chr14: 99,185,443-99,185,807 , GRCh37.p13 chr14: 99,651,780-99,652,144 BCL11B
    nsv4991331copy number variation1nstd200human GRCh38 chr14: 99,223,792-99,224,543 , GRCh37.p13 chr14: 99,690,129-99,690,880 BCL11B
    nsv4991330copy number variation1nstd200human GRCh38 chr14: 99,188,324-99,188,450 , GRCh37.p13 chr14: 99,654,661-99,654,787 BCL11B
    nsv4729352copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,538,014-100,082,239 , GRCh38.p12 chr14: 99,071,677-99,615,902 SETD3, RNU6-91P, 8 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4671541copy number variation1nstd186human GRCh37 chr14: 99,734,901-99,742,500 , GRCh38.p12 chr14: 99,268,564-99,276,163 BCL11B
    nsv4670791copy number variation1nstd186human GRCh37 chr14: 99,637,801-99,642,600 , GRCh38.p12 chr14: 99,171,464-99,176,263 BCL11B
    nsv4633509copy number variation1nstd183human GRCh37 chr14: 99,640,536-99,642,292 , GRCh38.p12 chr14: 99,174,199-99,175,955 BCL11B
    nsv4623906copy number variation1nstd183human GRCh37 chr14: 99,734,901-99,742,500 , GRCh38.p12 chr14: 99,268,564-99,276,163 BCL11B
    nsv4620333copy number variation1nstd183human GRCh37 chr14: 99,637,801-99,642,600 , GRCh38.p12 chr14: 99,171,464-99,176,263 BCL11B
    nsv4546453insertion1nstd166human GRCh37.p13 chr14: 99,689,173-99,689,173 , GRCh38.p12 chr14: 99,222,836-99,222,836 BCL11B
    nsv4530208copy number variation1nstd166human GRCh37.p13 chr14: 99,651,800-99,652,115 , GRCh38.p12 chr14: 99,185,463-99,185,778 BCL11B
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