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Items: 1 to 20 of 254

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969606inversion1nstd209human GRCh38 chr8: 23,219,486-23,319,833 , GRCh37.p13 chr8: 23,076,999-23,177,346 , LOXL2, 4 more genes
    nsv5924879copy number variation1nstd209human GRCh38 chr8: 23,225,576-23,227,787 , GRCh37.p13 chr8: 23,083,089-23,085,300 TNFRSF10A, TNFRSF10A-DT
    nsv5859377copy number variation1nstd209human GRCh38 chr8: 23,163,559-23,195,880 , GRCh37.p13 chr8: 23,021,072-23,053,393 TNFRSF10D, TNFRSF10A
    nsv5711034mobile element insertion2nstd211human GRCh38 chr8: 23,222,510-23,222,510 , GRCh37.p13 chr8: 23,080,023-23,080,023 TNFRSF10A
    nsv5561895sequence alteration1nstd206human GRCh38 chr8: 23,119,138-23,219,486 , GRCh37.p13 chr8: 22,976,651-23,076,999 TNFRSF10D, TNFRSF10A, 1 more genes
    nsv5488476copy number variation1nstd206human GRCh38 chr8: 23,211,646-23,211,788 , GRCh37.p13 chr8: 23,069,159-23,069,301 TNFRSF10A
    nsv5486911copy number variation1nstd206human GRCh38 chr8: 23,198,341-23,199,110 , GRCh37.p13 chr8: 23,055,854-23,056,623 TNFRSF10A
    nsv5481845copy number variation1nstd206human GRCh38 chr8: 23,163,003-23,196,275 , GRCh37.p13 chr8: 23,020,516-23,053,788 TNFRSF10D, TNFRSF10A
    nsv5395946mobile element insertion1nstd206human GRCh38 chr8: 23,222,510-23,222,561 , GRCh37.p13 chr8: 23,080,023-23,080,074 TNFRSF10A
    nsv5386157copy number variation2nstd186human GRCh37 chr8: 23,083,089-23,085,331 , GRCh38.p12 chr8: 23,225,576-23,227,818 TNFRSF10A-DT, TNFRSF10A
    nsv5308869copy number variation1nstd204human GRCh38.p13 chr8: 23,225,572-23,227,827 , GRCh37.p13 chr8: 23,083,085-23,085,340 TNFRSF10A-DT, TNFRSF10A
    nsv5241904copy number variation1nstd204human GRCh38.p13 chr8: 23,225,544-23,227,643 , GRCh37.p13 chr8: 23,083,057-23,085,156 TNFRSF10A, TNFRSF10A-DT
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5119889mobile element insertion1nstd203human GRCh38 chr8: 23,213,553-23,213,593 , GRCh37.p13 chr8: 23,071,066-23,071,106 TNFRSF10A
    nsv5116535mobile element insertion1nstd203human GRCh38 chr8: 23,220,912-23,220,927 , GRCh37.p13 chr8: 23,078,425-23,078,440 TNFRSF10A
    nsv5114221mobile element insertion1nstd203human GRCh38 chr8: 23,213,436-23,213,465 , GRCh37.p13 chr8: 23,070,949-23,070,978 TNFRSF10A
    nsv5106424mobile element insertion1nstd203human GRCh38 chr8: 23,213,554-23,213,592 , GRCh37.p13 chr8: 23,071,067-23,071,105 TNFRSF10A
    nsv5101314mobile element insertion1nstd203human GRCh38 chr8: 23,213,560-23,213,595 , GRCh37.p13 chr8: 23,071,073-23,071,108 TNFRSF10A
    nsv5100565mobile element insertion1nstd203human GRCh38 chr8: 23,213,443-23,213,465 , GRCh37.p13 chr8: 23,070,956-23,070,978 TNFRSF10A
    nsv4959685copy number variation1nstd200human GRCh38 chr8: 23,225,570-23,227,417 , GRCh37.p13 chr8: 23,083,083-23,084,930 TNFRSF10A, TNFRSF10A-DT
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