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Items: 1 to 20 of 760

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967430insertion1nstd209human GRCh38 chr3: 81,655,169-81,655,169 , GRCh37.p13 chr3: 81,704,320-81,704,320 GBE1
    nsv5964138insertion1nstd209human GRCh38 chr3: 81,721,232-81,721,232 , GRCh37.p13 chr3: 81,770,383-81,770,383 GBE1
    nsv5906221copy number variation1nstd209human GRCh38 chr3: 81,504,276-81,504,343 , GRCh37.p13 chr3: 81,553,427-81,553,494 GBE1
    nsv5904862copy number variation1nstd209human GRCh38 chr3: 81,750,622-81,750,671 , GRCh37.p13 chr3: 81,799,773-81,799,822 GBE1
    nsv5897367copy number variation1nstd209human GRCh38 chr3: 81,505,418-81,512,289 , GRCh37.p13 chr3: 81,554,569-81,561,440 GBE1, RNU2-28P
    nsv5896335copy number variation1nstd209human GRCh38 chr3: 81,737,363-81,737,412 , GRCh37.p13 chr3: 81,786,514-81,786,563 GBE1
    nsv5894011copy number variation1nstd209human GRCh38 chr3: 81,546,418-81,550,513 , GRCh37.p13 chr3: 81,595,569-81,599,664 GBE1
    nsv5889433copy number variation1nstd209human GRCh38 chr3: 81,527,329-81,527,434 , GRCh37.p13 chr3: 81,576,480-81,576,585 GBE1
    nsv5836837copy number variation1nstd209human GRCh38 chr3: 81,546,478-81,550,530 , GRCh37.p13 chr3: 81,595,629-81,599,681 GBE1
    nsv5836836copy number variation1nstd209human GRCh38 chr3: 81,505,046-81,512,328 , GRCh37.p13 chr3: 81,554,197-81,561,479 RNU2-28P, GBE1
    nsv5730962mobile element insertion1nstd211human GRCh38 chr3: 81,664,838-81,664,838 , GRCh37.p13 chr3: 81,713,989-81,713,989 GBE1
    nsv5714355mobile element insertion2nstd211human GRCh38 chr3: 81,721,235-81,721,235 , GRCh37.p13 chr3: 81,770,386-81,770,386 GBE1
    nsv5693736mobile element insertion1nstd211human GRCh38 chr3: 81,510,890-81,510,890 , GRCh37.p13 chr3: 81,560,041-81,560,041 GBE1
    nsv5692939mobile element insertion1nstd211human GRCh38 chr3: 81,673,791-81,673,791 , GRCh37.p13 chr3: 81,722,942-81,722,942 GBE1
    nsv5689495mobile element insertion1nstd211human GRCh38 chr3: 81,744,606-81,744,606 , GRCh37.p13 chr3: 81,793,757-81,793,757 GBE1
    nsv5682490mobile element insertion2nstd211human GRCh38 chr3: 81,644,553-81,644,553 , GRCh37.p13 chr3: 81,693,704-81,693,704 GBE1
    nsv5679413mobile element insertion1nstd211human GRCh38 chr3: 81,676,759-81,676,759 , GRCh37.p13 chr3: 81,725,910-81,725,910 GBE1
    nsv5673733copy number variation1nstd102humanPathogenic GRCh37 chr3: 81,810,516-81,810,678 , GRCh38.p12 chr3: 81,761,365-81,761,527 GBE1
    nsv5673732copy number variation1nstd102humanPathogenic GRCh37 chr3: 81,627,056-81,810,688 , GRCh38.p12 chr3: 81,577,905-81,761,537 SETP6, GBE1
    nsv5673731copy number variation1nstd102humanPathogenic GRCh37 chr3: 81,539,548-81,754,774 , GRCh38.p12 chr3: 81,490,397-81,705,623 GBE1, SETP6, 1 more genes
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