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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057753inversion1nstd229human GRCh38 chr3: 139,111,416-139,132,287 , GRCh37.p13 chr3: 138,830,258-138,851,129 BPESC1
    nsv7057723inversion1nstd229human GRCh38 chr3: 139,122,337-139,142,772 , GRCh37.p13 chr3: 138,841,179-138,861,614 BPESC1
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6738014copy number variation1nstd229human GRCh38 chr3: 138,480,262-139,118,462 , GRCh37.p13 chr3: 138,199,104-138,837,304 GAPDHP39, ATP5MC1P3, 15 more genes
    nsv6737340copy number variation1nstd229human GRCh38 chr3: 139,120,147-139,184,690 , GRCh37.p13 chr3: 138,838,989-138,903,532 BPESC1
    nsv6729872copy number variation1nstd229human GRCh38 chr3: 139,117,101-139,138,200 , GRCh37.p13 chr3: 138,835,943-138,857,042 BPESC1
    nsv6725094copy number variation1nstd229human GRCh38 chr3: 138,618,667-140,093,940 , GRCh37.p13 chr3: 138,337,509-139,812,782 RPL23AP40, FOXL2NB, 25 more genes
    nsv6722699copy number variation1nstd229human GRCh38 chr3: 139,101,044-139,103,584 , GRCh37.p13 chr3: 138,819,886-138,822,426 BPESC1
    nsv6720918copy number variation1nstd229human GRCh38 chr3: 138,441,482-139,164,353 , GRCh37.p13 chr3: 138,160,324-138,883,195 FAIM, ATP5MC1P3, 15 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6571021inversion1nstd223human GRCh38 chr3: 139,114,323-139,114,379 , GRCh37.p13 chr3: 138,833,165-138,833,221 BPESC1
    nsv6374232copy number variation1nstd223human GRCh38 chr3: 139,120,901-139,121,800 , GRCh37.p13 chr3: 138,839,743-138,840,642 BPESC1
    nsv6365014copy number variation1nstd223human GRCh38 chr3: 139,112,229-139,112,856 , GRCh37.p13 chr3: 138,831,071-138,831,698 BPESC1
    nsv6362129copy number variation1nstd223human GRCh38 chr3: 138,618,667-140,093,940 , GRCh37.p13 chr3: 138,337,509-139,812,782 RBP2, FAIM, 25 more genes
    nsv6360795copy number variation1nstd223human GRCh38 chr3: 139,106,403-139,107,180 , GRCh37.p13 chr3: 138,825,245-138,826,022 BPESC1
    nsv6311778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,781,658-139,258,560 , GRCh38.p12 chr3: 138,062,816-139,539,718 PRR23C, ACTG1P1, 29 more genes
    nsv6254736mobile element insertion1nstd215human GRCh38 chr3: 139,117,577-139,117,577 , GRCh37.p13 chr3: 138,836,419-138,836,419 BPESC1
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    nsv6074726insertion1nstd212human GRCh38 chr3: 139,114,539-139,114,539 , GRCh37.p13 chr3: 138,833,381-138,833,381 BPESC1
    nsv6072115insertion1nstd212human GRCh38 chr3: 139,115,850-139,115,850 , GRCh37.p13 chr3: 138,834,692-138,834,692 BPESC1
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