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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969646insertion1nstd209human GRCh38 chr12: 9,606,707-9,606,707 , GRCh37.p13 chr12: 9,759,303-9,759,303 , KLRB1
    nsv5918807copy number variation1nstd209human GRCh38 chr12: 9,603,709-9,613,533 , GRCh37.p13 chr12: 9,756,305-9,766,129 , KLRB1
    nsv5853441copy number variation1nstd209human GRCh38 chr12: 9,603,758-9,613,526 , GRCh37.p13 chr12: 9,756,354-9,766,122 , KLRB1
    nsv5852622copy number variation2nstd209human GRCh38 chr12: 9,606,770-9,608,189 , GRCh37.p13 chr12: 9,759,366-9,760,785 , KLRB1
    nsv5702075mobile element insertion1nstd211human GRCh38 chr12: 9,594,024-9,594,024 , GRCh37.p13 chr12: 9,746,620-9,746,620 KLRB1
    nsv5653977insertion1nstd207human GRCh38 chr12: 9,607,335-9,607,335 , GRCh37.p13 chr12: 9,759,931-9,759,931 , KLRB1
    nsv5548345insertion1nstd206human GRCh38 chr12: 9,592,709-9,592,709 , GRCh37.p13 chr12: 9,745,305-9,745,305 KLRB1
    nsv5504091copy number variation1nstd206human GRCh38 chr12: 9,603,579-9,613,534 , GRCh37.p13 chr12: 9,756,175-9,766,130 , KLRB1
    nsv5432689mobile element insertion1nstd206human GRCh38 chr12: 9,594,024-9,594,075 , GRCh37.p13 chr12: 9,746,620-9,746,671 KLRB1
    nsv5373977translocation1nstd200human GRCh38 chr12: 9,603,711-9,603,711 , GRCh38 chr12: 9,613,534-9,613,534 , GRCh37.p13 chr12: 9,756,307-9,756,307 , GRCh37.p13 chr12: 9,766,130-9,766,130 , KLRB1
    nsv5333701translocation1nstd200human GRCh37 chr12: 9,766,130-9,766,130 , GRCh37 chr12: 9,756,307-9,756,307 , GRCh38.p12 chr12: 9,603,711-9,603,711 , GRCh38.p12 chr12: 9,613,534-9,613,534 , KLRB1
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5303453copy number variation1nstd204human GRCh37.p13 chr12: 9,720,241-9,782,365 , GRCh38.p13 chr12: 9,567,645-9,629,769 , KLRB1, 3 more genes
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4974327copy number variation1nstd200human GRCh38 chr12: 9,411,203-9,658,005 , GRCh37.p13 chr12: 9,563,799-9,810,601 , LOC374443, 8 more genes
    nsv4972162copy number variation1nstd200human GRCh38 chr12: 9,567,653-9,629,764 , GRCh37.p13 chr12: 9,720,249-9,782,360 , LOC374443, 3 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4830186copy number variation1nstd200human GRCh37 chr12: 9,720,249-9,782,360 , GRCh38.p12 chr12: 9,567,653-9,629,764 , LOC374443, 3 more genes
    nsv4733421copy number variation1nstd199human GRCh37 chr12: 9,759,265-9,759,321 , GRCh38.p12 chr12: 9,606,669-9,606,725 , KLRB1
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
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