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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120406copy number variation1nstd186human GRCh37 chr2: 111,883,194-111,886,097 , GRCh38.p12 chr2: 111,125,617-111,128,520 BCL2L11
    nsv5963104insertion1nstd209human GRCh38 chr2: 111,147,347-111,147,347 , GRCh37.p13 chr2: 111,904,924-111,904,924 BCL2L11
    nsv5873161copy number variation1nstd209human GRCh38 chr2: 111,160,722-111,160,851 , GRCh37.p13 chr2: 111,918,299-111,918,428 BCL2L11
    nsv5872861copy number variation1nstd209human GRCh38 chr2: 111,125,617-111,128,519 , GRCh37.p13 chr2: 111,883,194-111,886,096 BCL2L11
    nsv5831167copy number variation1nstd209human GRCh38 chr2: 111,125,552-111,128,474 , GRCh37.p13 chr2: 111,883,129-111,886,051 BCL2L11
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5447935copy number variation1nstd206human GRCh38 chr2: 111,129,000-111,129,139 , GRCh37.p13 chr2: 111,886,577-111,886,716 BCL2L11
    nsv5437080copy number variation1nstd206human GRCh38 chr2: 111,125,617-111,128,520 , GRCh37.p13 chr2: 111,883,194-111,886,097 BCL2L11
    nsv5344727translocation1nstd200human GRCh37 chr2: 111,886,097-111,886,097 , GRCh37 chr2: 111,883,194-111,883,194 , GRCh38.p12 chr2: 111,125,617-111,125,617 , GRCh38.p12 chr2: 111,128,520-111,128,520 BCL2L11
    nsv5291329copy number variation1nstd204human GRCh38.p13 chr2: 111,160,718-111,160,857 , GRCh37.p13 chr2: 111,918,295-111,918,434 BCL2L11
    nsv5287975copy number variation1nstd204human GRCh38.p13 chr2: 111,125,607-111,128,522 , GRCh37.p13 chr2: 111,883,184-111,886,099 BCL2L11
    nsv5220042copy number variation1nstd204human GRCh38.p13 chr2: 111,125,577-111,128,149 , GRCh37.p13 chr2: 111,883,154-111,885,726 BCL2L11
    nsv5206252copy number variation1nstd204human GRCh38.p13 chr2: 111,125,601-111,128,500 , GRCh37.p13 chr2: 111,883,178-111,886,077 BCL2L11
    nsv5205524copy number variation1nstd204human GRCh38.p13 chr2: 111,143,277-111,144,526 , GRCh37.p13 chr2: 111,900,854-111,902,103 BCL2L11
    nsv5204192copy number variation1nstd204human GRCh38.p13 chr2: 111,101,689-111,138,794 , GRCh37.p13 chr2: 111,859,266-111,896,371 ACOXL, BCL2L11, 1 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4915026copy number variation1nstd200human GRCh38 chr2: 111,160,722-111,160,854 , GRCh37.p13 chr2: 111,918,299-111,918,431 BCL2L11
    nsv4915025copy number variation1nstd200human GRCh38 chr2: 111,159,047-111,161,927 , GRCh37.p13 chr2: 111,916,624-111,919,504 BCL2L11
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