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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129489insertion1nstd186human GRCh37 chr22: 40,352,644-40,352,680 , GRCh38.p12 chr22: 39,956,640-39,956,676 GRAP2
    nsv5975461insertion1nstd209human GRCh38 chr22: 39,956,636-39,956,636 , GRCh37.p13 chr22: 40,352,640-40,352,640 GRAP2
    nsv5956633copy number variation1nstd209human GRCh38 chr22: 39,898,611-39,899,780 , GRCh37.p13 chr22: 40,294,615-40,295,784 GRAP2
    nsv5701275mobile element insertion1nstd211human GRCh38 chr22: 39,964,734-39,964,734 , GRCh37.p13 chr22: 40,360,738-40,360,738 GRAP2, TMA7B
    nsv5696014mobile element insertion1nstd211human GRCh38 chr22: 39,909,026-39,909,026 , GRCh37.p13 chr22: 40,305,030-40,305,030 GRAP2
    nsv5553178copy number variation1nstd206human GRCh38 chr22: 39,911,360-39,915,275 , GRCh37.p13 chr22: 40,307,364-40,311,279 GRAP2
    nsv5544329insertion1nstd206human GRCh38 chr22: 39,956,640-39,956,676 , GRCh37.p13 chr22: 40,352,644-40,352,680 GRAP2
    nsv5538388copy number variation1nstd206human GRCh38 chr22: 39,968,164-39,968,234 , GRCh37.p13 chr22: 40,364,168-40,364,238 GRAP2
    nsv5414057mobile element insertion1nstd206human GRCh38 chr22: 39,909,026-39,909,077 , GRCh37.p13 chr22: 40,305,030-40,305,081 GRAP2
    nsv5360587translocation1nstd200human GRCh38 chr22: 39,927,919-39,927,919 , GRCh38 chr22: 39,927,836-39,927,836 , GRCh37.p13 chr22: 40,323,840-40,323,840 , GRCh37.p13 chr22: 40,323,923-40,323,923 GRAP2
    nsv5360586translocation1nstd200human GRCh38 chr22: 39,915,275-39,915,275 , GRCh38 chr22: 39,911,359-39,911,359 , GRCh37.p13 chr22: 40,307,363-40,307,363 , GRCh37.p13 chr22: 40,311,279-40,311,279 GRAP2
    nsv5171927mobile element insertion1nstd203human GRCh38 chr22: 39,955,794-39,955,802 , GRCh37.p13 chr22: 40,351,798-40,351,806 GRAP2
    nsv5170031mobile element insertion1nstd203human GRCh38 chr22: 39,911,755-39,911,764 , GRCh37.p13 chr22: 40,307,759-40,307,768 GRAP2
    nsv5163184mobile element insertion1nstd203human GRCh38 chr22: 39,956,636-39,956,640 , GRCh37.p13 chr22: 40,352,640-40,352,644 GRAP2
    nsv5040338copy number variation1nstd200human GRCh38 chr22: 39,934,303-39,935,255 , GRCh37.p13 chr22: 40,330,307-40,331,259 GRAP2
    nsv5037355copy number variation1nstd200human GRCh38 chr22: 39,922,279-39,922,479 , GRCh37.p13 chr22: 40,318,283-40,318,483 GRAP2
    nsv4870416copy number variation1nstd200human GRCh37 chr22: 40,307,364-40,311,279 , GRCh38.p12 chr22: 39,911,360-39,915,275 GRAP2
    nsv4766730insertion1nstd199human GRCh37 chr22: 40,352,630-40,352,630 , GRCh38.p12 chr22: 39,956,626-39,956,626 GRAP2
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
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