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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973665insertion1nstd209human GRCh38 chr11: 61,861,353-61,861,353 , GRCh37.p13 chr11: 61,628,825-61,628,825 FADS2
    nsv5922208copy number variation1nstd209human GRCh38 chr11: 61,815,124-61,815,180 , GRCh37.p13 chr11: 61,582,596-61,582,652 FADS1, FADS2, 1 more genes
    nsv5851041copy number variation2nstd209human GRCh38 chr11: 61,816,293-61,817,335 , GRCh37.p13 chr11: 61,583,765-61,584,807 FADS1, FADS2
    nsv5717718mobile element insertion2nstd211human GRCh38 chr11: 61,817,851-61,817,851 , GRCh37.p13 chr11: 61,585,323-61,585,323 FADS2
    nsv5704776mobile element insertion1nstd211human GRCh38 chr11: 61,818,251-61,818,251 , GRCh37.p13 chr11: 61,585,723-61,585,723 FADS2
    nsv5663702insertion1nstd207human GRCh38 chr11: 61,824,502-61,824,502 , GRCh37.p13 chr11: 61,591,974-61,591,974 FADS2
    nsv5563667sequence alteration1nstd206human GRCh38 chr11: 61,852,830-61,853,293 , GRCh37.p13 chr11: 61,620,302-61,620,765 FADS2
    nsv5544210insertion1nstd206human GRCh38 chr11: 61,820,769-61,820,886 , GRCh37.p13 chr11: 61,588,241-61,588,358 FADS2
    nsv5541581insertion1nstd206human GRCh38 chr11: 61,852,833-61,852,833 , GRCh37.p13 chr11: 61,620,305-61,620,305 FADS2
    nsv5503897copy number variation1nstd206human GRCh38 chr11: 61,815,230-61,815,282 , GRCh37.p13 chr11: 61,582,702-61,582,754 FADS2, FADS1, 1 more genes
    nsv5413412mobile element insertion1nstd206human GRCh38 chr11: 61,818,251-61,818,302 , GRCh37.p13 chr11: 61,585,723-61,585,774 FADS2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373655translocation1nstd200human GRCh38 chr11: 61,852,833-61,852,833 , GRCh38 chr11: 61,853,293-61,853,293 , GRCh37.p13 chr11: 61,620,765-61,620,765 , GRCh37.p13 chr11: 61,620,305-61,620,305 FADS2
    nsv5345478translocation1nstd200human GRCh37 chr11: 61,620,305-61,620,305 , GRCh37 chr11: 61,620,765-61,620,765 , GRCh38.p12 chr11: 61,852,833-61,852,833 , GRCh38.p12 chr11: 61,853,293-61,853,293 FADS2
    nsv5327964translocation1nstd204human GRCh38.p13 chr11: 61,853,293-61,853,293 , GRCh38.p13 chr11: 61,852,833-61,852,833 , GRCh37.p13 chr11: 61,620,765-61,620,765 , GRCh37.p13 chr11: 61,620,305-61,620,305 FADS2
    nsv5131198mobile element insertion1nstd203human GRCh38 chr11: 61,861,353-61,861,366 , GRCh37.p13 chr11: 61,628,825-61,628,838 FADS2
    nsv5129640mobile element insertion1nstd203human GRCh38 chr11: 61,818,235-61,818,235 , GRCh37.p13 chr11: 61,585,707-61,585,707 FADS2
    nsv4985000copy number variation1nstd200human GRCh38 chr11: 61,849,067-61,852,599 , GRCh37.p13 chr11: 61,616,539-61,620,071 FADS2
    nsv4979662copy number variation1nstd200human GRCh38 chr11: 61,858,463-61,859,295 , GRCh37.p13 chr11: 61,625,935-61,626,767 FADS2
    nsv4979661copy number variation1nstd200human GRCh38 chr11: 61,843,798-61,847,023 , GRCh37.p13 chr11: 61,611,270-61,614,495 FADS2
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