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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889723copy number variation1nstd209human GRCh38 chr2: 181,491,244-181,491,558 , GRCh37.p13 chr2: 182,355,971-182,356,285 ITGA4
    nsv5721240mobile element insertion1nstd211human GRCh38 chr2: 181,503,300-181,503,300 , GRCh37.p13 chr2: 182,368,027-182,368,027 ITGA4
    nsv5685956mobile element insertion2nstd211human GRCh38 chr2: 181,469,283-181,469,283 , GRCh37.p13 chr2: 182,334,010-182,334,010 ITGA4
    nsv5567036copy number variation1nstd207human GRCh38 chr2: 181,491,244-181,491,558 , GRCh37.p13 chr2: 182,355,971-182,356,285 ITGA4
    nsv5563140mobile element insertion1nstd206human GRCh38 chr2: 181,503,300-181,503,351 , GRCh37.p13 chr2: 182,368,027-182,368,078 ITGA4
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452588copy number variation1nstd206human GRCh38 chr2: 181,491,256-181,491,559 , GRCh37.p13 chr2: 182,355,983-182,356,286 ITGA4
    nsv5444205copy number variation1nstd206human GRCh38 chr2: 181,535,912-181,535,990 , GRCh37.p13 chr2: 182,400,639-182,400,717 CERKL, ITGA4
    nsv5439356copy number variation1nstd206human GRCh38 chr2: 181,535,008-181,535,094 , GRCh37.p13 chr2: 182,399,735-182,399,821 ITGA4, CERKL
    nsv5399967mobile element insertion1nstd206human GRCh38 chr2: 181,469,283-181,469,334 , GRCh37.p13 chr2: 182,334,010-182,334,061 ITGA4
    nsv5385193mobile element deletion2nstd186human GRCh37 chr2: 182,355,983-182,356,286 , GRCh38.p12 chr2: 181,491,256-181,491,559 ITGA4
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
    nsv5219187mobile element deletion1nstd204human GRCh38.p13 chr2: 181,491,256-181,491,559 , GRCh37.p13 chr2: 182,355,983-182,356,286 ITGA4
    nsv5214355copy number variation1nstd204human GRCh38.p13 chr2: 181,491,301-181,491,500 , GRCh37.p13 chr2: 182,356,028-182,356,227 ITGA4
    nsv5079346mobile element insertion1nstd203human GRCh38 chr2: 181,460,711-181,460,722 , GRCh37.p13 chr2: 182,325,438-182,325,449 ITGA4
    nsv5072083mobile element insertion1nstd203human GRCh38 chr2: 181,480,536-181,480,553 , GRCh37.p13 chr2: 182,345,263-182,345,280 ITGA4
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv5029942inversion1nstd200human GRCh38 chr2: 181,253,377-181,757,405 , GRCh37.p13 chr2: 182,118,104-182,622,132 ITGA4, NEUROD1, 5 more genes
    nsv4909933copy number variation1nstd200human GRCh38 chr2: 181,535,008-181,535,094 , GRCh37.p13 chr2: 182,399,735-182,399,821 CERKL, ITGA4
    nsv4909932copy number variation1nstd200human GRCh38 chr2: 181,475,297-181,482,831 , GRCh37.p13 chr2: 182,340,024-182,347,558 ITGA4
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