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Items: 1 to 20 of 582

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098723copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,681,152-107,783,055 , GRCh38.p12 chrX: 108,437,922-108,539,825 COL4A5, COL4A6
    nsv7098490copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,920,710-107,930,944 , GRCh38.p12 chrX: 108,677,480-108,687,714 COL4A5
    nsv7098489copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,858,121-107,979,574 , GRCh38.p12 chrX: 108,614,891-108,736,344 IRS4-AS1, IRS4, 1 more genes
    nsv7098488copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,849,932-107,858,274 , GRCh38.p12 chrX: 108,606,702-108,615,044 COL4A5
    nsv7098487copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,834,471-107,835,925 , GRCh38.p12 chrX: 108,591,241-108,592,695 COL4A5
    nsv7098486copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,807,092-107,898,707 , GRCh38.p12 chrX: 108,563,862-108,655,477 COL4A5
    nsv7098485copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,802,274-107,933,678 , GRCh38.p12 chrX: 108,559,044-108,690,448 COL4A5
    nsv7098484copy number variation1nstd102humanUncertain significance GRCh37 chrX: 107,682,568-107,683,456 , GRCh38.p12 chrX: 108,439,338-108,440,226 COL4A5, COL4A6
    nsv7098213copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,898,541-107,979,574 , GRCh38.p12 chrX: 108,655,311-108,736,344 COL4A5, IRS4, 1 more genes
    nsv7098212copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,819,120-107,827,775 , GRCh38.p12 chrX: 108,575,890-108,584,545 COL4A5
    nsv7098211copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,817,240-107,821,596 , GRCh38.p12 chrX: 108,574,010-108,578,366 COL4A5
    nsv7098210copy number variation1nstd102humanUncertain significance GRCh37 chrX: 107,400,230-107,939,608 , GRCh38.p12 chrX: 108,157,000-108,696,378 COL4A6, COL4A5
    nsv7098109copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 107,819,120-107,820,077 , GRCh38.p12 chrX: 108,575,890-108,576,847 COL4A5
    nsv7098107copy number variation1nstd102humanPathogenic GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020 VSIG1, NXT2, 32 more genes
    nsv7097979copy number variation1nstd102humanUncertain significance GRCh37 chrX: 107,930,692-107,930,944 , GRCh38.p12 chrX: 108,687,462-108,687,714 COL4A5
    nsv7097978copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,908,717-107,911,754 , GRCh38.p12 chrX: 108,665,487-108,668,524 COL4A5
    nsv7097977copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,867,446-107,869,599 , GRCh38.p12 chrX: 108,624,216-108,626,369 COL4A5
    nsv7097976copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 107,782,956-107,898,707 , GRCh38.p12 chrX: 108,539,726-108,655,477 COL4A5
    nsv7093340copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 107,841,959-107,842,012 , GRCh38 chrX: 108,598,729-108,598,782 COL4A5
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