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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5613983insertion1nstd207human GRCh38 chr1: 111,755,128-111,755,128 , GRCh37.p13 chr1: 112,297,750-112,297,750 DDX20, INKA2, 1 more genes
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5288187copy number variation1nstd204human GRCh37.p13 chr1: 112,286,286-112,288,490 , GRCh38.p13 chr1: 111,743,664-111,745,868 INKA2, INKA2-AS1, 1 more genes
    nsv5211734copy number variation1nstd204human GRCh38.p13 chr1: 111,743,562-111,746,321 , GRCh37.p13 chr1: 112,286,184-112,288,943 INKA2-AS1, INKA2, 1 more genes
    nsv5202432copy number variation1nstd204human GRCh38.p13 chr1: 111,743,701-111,745,900 , GRCh37.p13 chr1: 112,286,323-112,288,522 INKA2, LOC101928718, 1 more genes
    nsv4890781copy number variation1nstd200human GRCh38 chr1: 111,753,044-111,754,444 , GRCh37.p13 chr1: 112,295,666-112,297,066 LOC101928718, INKA2, 1 more genes
    nsv4890780copy number variation1nstd200human GRCh38 chr1: 111,743,668-111,745,866 , GRCh37.p13 chr1: 112,286,290-112,288,488 INKA2, INKA2-AS1, 1 more genes
    nsv4773682copy number variation1nstd200human GRCh37 chr1: 112,295,666-112,297,066 , GRCh38.p12 chr1: 111,753,044-111,754,444 DDX20, INKA2, 1 more genes
    nsv4773681copy number variation1nstd200human GRCh37 chr1: 112,286,290-112,288,488 , GRCh38.p12 chr1: 111,743,668-111,745,866 INKA2, LOC101928718, 1 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4764539insertion1nstd199human GRCh38.p12 chr1: 111,755,141-111,755,141 , GRCh37 chr1: 112,297,763-112,297,763 DDX20, INKA2, 1 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4454547copy number variation1nstd102humanPathogenic GRCh37 chr1: 110,994,179-112,360,446 , GRCh38.p12 chr1: 110,451,557-111,817,824 CCNT2P1, PROK1, 44 more genes
    nsv4330538inversion1nstd166human GRCh37.p13 chr1: 94,223,082-113,632,613 , GRCh38.p12 chr1: 93,757,526-113,089,991 , AMPD2, 329 more genes
    nsv4072287copy number variation1nstd166human GRCh37.p13 chr1: 112,295,666-112,297,066 , GRCh38.p12 chr1: 111,753,044-111,754,444 LOC101928718, DDX20, 1 more genes
    nsv4064647copy number variation1nstd166human GRCh37.p13 chr1: 112,297,729-112,297,808 , GRCh38.p12 chr1: 111,755,107-111,755,186 DDX20, INKA2, 1 more genes
    nsv3920130copy number variation1nstd102humanPathogenic NCBI36 chr1: 103,429,843-112,252,782 , GRCh37.p13 chr1: 103,657,255-112,451,259 , GRCh38.p12 chr1: 103,191,699-111,908,637 LOC105378898, LOC105378901, 166 more genes
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