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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901165copy number variation1nstd209human GRCh38 chr3: 182,883,479-182,883,543 , GRCh37.p13 chr3: 182,601,267-182,601,331 ATP11B
    nsv5895433copy number variation1nstd209human GRCh38 chr3: 182,847,543-182,847,700 , GRCh37.p13 chr3: 182,565,331-182,565,488 ATP11B
    nsv5716383mobile element insertion1nstd211human GRCh38 chr3: 182,835,612-182,835,612 , GRCh37.p13 chr3: 182,553,400-182,553,400 ATP11B
    nsv5688785mobile element insertion1nstd211human GRCh38 chr3: 182,855,104-182,855,104 , GRCh37.p13 chr3: 182,572,892-182,572,892 ATP11B
    nsv5682188mobile element insertion1nstd211human GRCh38 chr3: 182,921,780-182,921,780 , GRCh37.p13 chr3: 182,639,568-182,639,568 ATP11B
    nsv5676662mobile element insertion1nstd211human GRCh38 chr3: 182,903,961-182,903,961 , GRCh37.p13 chr3: 182,621,749-182,621,749 ATP11B
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5450080copy number variation1nstd206human GRCh38 chr3: 182,883,481-182,883,544 , GRCh37.p13 chr3: 182,601,269-182,601,332 ATP11B
    nsv5447306copy number variation1nstd206human GRCh38 chr3: 182,823,397-182,823,890 , GRCh37.p13 chr3: 182,541,185-182,541,678 ATP11B
    nsv5435475copy number variation1nstd206human GRCh38 chr3: 182,874,783-182,874,844 , GRCh37.p13 chr3: 182,592,571-182,592,632 ATP11B
    nsv5411203mobile element insertion1nstd206human GRCh38 chr3: 182,903,961-182,904,012 , GRCh37.p13 chr3: 182,621,749-182,621,800 ATP11B
    nsv5404585mobile element insertion1nstd206human GRCh38 chr3: 182,855,104-182,855,149 , GRCh37.p13 chr3: 182,572,892-182,572,937 ATP11B
    nsv5397589mobile element insertion1nstd206human GRCh38 chr3: 182,921,780-182,921,831 , GRCh37.p13 chr3: 182,639,568-182,639,619 ATP11B
    nsv5377592translocation1nstd200human GRCh38 chr3: 182,792,774-182,792,774 , GRCh38 chr3: 182,795,479-182,795,479 , GRCh37.p13 chr3: 182,510,562-182,510,562 , GRCh37.p13 chr3: 182,513,267-182,513,267 ATP11B, ATP11B-DT
    nsv5367226translocation1nstd200human GRCh38 chr3: 182,830,344-182,830,344 , GRCh38 chr3: 182,830,398-182,830,398 , GRCh37.p13 chr3: 182,548,132-182,548,132 , GRCh37.p13 chr3: 182,548,186-182,548,186 ATP11B
    nsv5352275translocation1nstd200human GRCh38 chr3: 182,922,339-182,922,339 , GRCh38 chr3: 182,922,265-182,922,265 , GRCh37.p13 chr3: 182,640,127-182,640,127 , GRCh37.p13 chr3: 182,640,053-182,640,053 ATP11B
    nsv5352273translocation1nstd200human GRCh38 chr3: 182,874,783-182,874,783 , GRCh38 chr3: 182,874,844-182,874,844 , GRCh37.p13 chr3: 182,592,632-182,592,632 , GRCh37.p13 chr3: 182,592,571-182,592,571 ATP11B
    nsv5352272translocation1nstd200human GRCh38 chr3: 182,795,226-182,795,226 , GRCh38 chr3: 182,792,773-182,792,773 , GRCh37.p13 chr3: 182,510,561-182,510,561 , GRCh37.p13 chr3: 182,513,014-182,513,014 ATP11B, ATP11B-DT
    nsv5337919translocation1nstd200human GRCh37 chr3: 182,592,632-182,592,632 , GRCh37 chr3: 182,592,571-182,592,571 , GRCh38.p12 chr3: 182,874,844-182,874,844 , GRCh38.p12 chr3: 182,874,783-182,874,783 ATP11B
    nsv5307492copy number variation1nstd204human GRCh38.p13 chr3: 182,824,055-182,840,514 , GRCh37.p13 chr3: 182,541,843-182,558,302 ATP11B
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