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Items: 1 to 20 of 1213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5978464insertion1nstd209human GRCh38 chr10: 133,536,531-133,536,531 , GRCh37.p13 chr10: 135,350,035-135,350,035 CYP2E1
    nsv5851852copy number variation1nstd209human GRCh38 chr10: 133,517,296-133,529,530 , GRCh37.p13 chr10: 135,330,800-135,343,034 , CYP2E1
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5505886copy number variation1nstd206human GRCh38 chr10: 133,426,565-133,573,130 , GRCh37.p13 chr10: 135,240,069-135,386,634 , SPRNP1, 8 more genes
    nsv5497134copy number variation1nstd206human GRCh38 chr10: 133,537,130-133,662,130 , GRCh37.p13 chr10: 135,350,634-135,475,634 CYP2E1, SYCE1, 6 more genes
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5310310copy number variation1nstd204human GRCh37.p13 chr10: 135,321,980-135,412,272 , GRCh38.p13 chr10: 133,508,476-133,598,768 , CYP2E1, 4 more genes
    nsv5260225copy number variation1nstd204human GRCh38.p13 chr10: 133,528,151-133,534,230 , GRCh37.p13 chr10: 135,341,655-135,347,734 CYP2E1
    nsv5258239copy number variation1nstd204human GRCh38.p13 chr10: 133,539,201-133,553,600 , GRCh37.p13 chr10: 135,352,705-135,367,104 SYCE1, CYP2E1
    nsv5256430copy number variation1nstd204human GRCh38.p13 chr10: 133,533,481-133,562,238 , GRCh37.p13 chr10: 135,346,985-135,375,742 SYCE1, CYP2E1
    nsv5255930copy number variation1nstd204human GRCh38.p13 chr10: 133,508,446-133,547,876 , GRCh37.p13 chr10: 135,321,950-135,361,380 , LOC105378575, 1 more genes
    nsv5250511copy number variation1nstd204human GRCh37.p13 chr10: 135,247,805-135,351,304 , GRCh38.p13 chr10: 133,434,301-133,537,800 , CYP2E1, 4 more genes
    nsv5248253copy number variation1nstd204human GRCh38.p13 chr10: 133,506,671-133,539,116 , GRCh37.p13 chr10: 135,320,175-135,352,620 , LOC105378575, 1 more genes
    nsv5245243copy number variation1nstd204human GRCh37.p13 chr10: 135,246,305-135,392,704 , GRCh38.p13 chr10: 133,432,801-133,579,200 , CYP2E1, 7 more genes
    nsv5245168copy number variation1nstd204human GRCh38.p13 chr10: 133,481,001-133,538,700 , GRCh37.p13 chr10: 135,294,505-135,352,204 , OR7M1P, 2 more genes
    nsv5240883copy number variation1nstd204human GRCh38.p13 chr10: 133,522,306-133,594,261 , GRCh37.p13 chr10: 135,335,810-135,407,765 , CYP2E1, 3 more genes
    nsv4984087copy number variation1nstd200human GRCh38 chr10: 133,517,920-133,601,163 , GRCh37.p13 chr10: 135,331,424-135,414,667 , OR6L1P, 3 more genes
    nsv4984086copy number variation1nstd200human GRCh38 chr10: 133,508,481-133,598,759 , GRCh37.p13 chr10: 135,321,985-135,412,263 , SPRNP1, 4 more genes
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