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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979049copy number variation1nstd209human GRCh38 chrX: 13,759,096-13,761,095 , GRCh37.p13 chrX: 13,777,215-13,779,214 OFD1
    nsv5978414copy number variation1nstd209human GRCh38 chrX: 13,723,218-13,773,881 , GRCh37.p13 chrX: 13,741,337-13,792,000 TRAPPC2, OFD1, 1 more genes
    nsv5972133copy number variation1nstd209human GRCh38 chrX: 13,747,196-13,749,695 , GRCh37.p13 chrX: 13,765,315-13,767,814 OFD1
    nsv5972068copy number variation1nstd209human GRCh38 chrX: 13,770,382-13,773,881 , GRCh37.p13 chrX: 13,788,501-13,792,000 OFD1, GPM6B
    nsv5725984mobile element insertion1nstd211human GRCh38 chrX: 13,745,893-13,745,893 , GRCh37.p13 chrX: 13,764,012-13,764,012 OFD1
    nsv5673899copy number variation1nstd102humanPathogenic GRCh37 chrX: 13,764,568-13,768,647 , GRCh38 chrX: 13,746,449-13,750,528 OFD1
    nsv5559869mobile element insertion1nstd206human GRCh38 chrX: 13,745,893-13,745,944 , GRCh37.p13 chrX: 13,764,012-13,764,063 OFD1
    nsv5433830copy number variation1nstd206human GRCh38 chrX: 13,761,780-13,761,928 , GRCh37.p13 chrX: 13,779,899-13,780,047 OFD1
    nsv5375887translocation1nstd200human GRCh38 chrX: 13,718,121-13,718,121 , GRCh38 chrX: 13,756,060-13,756,060 , GRCh37.p13 chrX: 13,774,179-13,774,179 , GRCh37.p13 chrX: 13,736,240-13,736,240 TRAPPC2, OFD1
    nsv5196946mobile element insertion1nstd203human GRCh38 chrX: 13,745,883-13,745,888 , GRCh37.p13 chrX: 13,764,002-13,764,007 OFD1
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905205copy number variation1nstd200human GRCh38 chrX: 13,543,258-13,796,069 , GRCh37.p13 chrX: 13,561,377-13,814,188 TCEANC, TRAPPC2, 9 more genes
    nsv4772512copy number variation1nstd200human GRCh37 chrX: 13,561,377-13,814,188 , GRCh38.p12 chrX: 13,543,258-13,796,069 OFD1, LOC107985657, 9 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728507copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 10,478,359-15,357,092 , GRCh38.p12 chrX: 10,510,319-15,338,970 AMELX, ARHGAP6, 49 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4682997copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 13,753,185-13,787,232 , GRCh38.p12 chrX: 13,735,066-13,769,113 GPM6B, TRAPPC2, 1 more genes
    nsv4674815copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-17,502,124 , GRCh38.p12 chrX: 251,879-17,484,001 PTMAP14, LOC100132857, 189 more genes
    nsv4674615copy number variation1nstd102humanPathogenic GRCh37 chrX: 1,240,318-20,986,848 , GRCh38.p12 chrX: 1,140,165-20,968,730 RNA5SP499, GS1-600G8.3, 217 more genes
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