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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975245insertion1nstd209human GRCh38 chr11: 22,824,498-22,824,498 , GRCh37.p13 chr11: 22,846,044-22,846,044 GAS2, SVIP
    nsv5698779mobile element insertion2nstd211human GRCh38 chr11: 22,827,815-22,827,815 , GRCh37.p13 chr11: 22,849,361-22,849,361 GAS2, SVIP
    nsv5660354insertion1nstd207human GRCh38 chr11: 22,824,452-22,824,452 , GRCh37.p13 chr11: 22,845,998-22,845,998 GAS2, SVIP
    nsv5495901copy number variation1nstd206human GRCh38 chr11: 22,813,734-23,250,368 , GRCh37.p13 chr11: 22,835,280-23,271,914 , GAS2, 3 more genes
    nsv5411558mobile element insertion1nstd206human GRCh38 chr11: 22,827,815-22,827,859 , GRCh37.p13 chr11: 22,849,361-22,849,405 GAS2, SVIP
    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
    nsv5135031mobile element insertion1nstd203human GRCh38 chr11: 22,827,815-22,827,815 , GRCh37.p13 chr11: 22,849,361-22,849,361 SVIP, GAS2
    nsv5132917mobile element insertion1nstd203human GRCh38 chr11: 22,827,810-22,827,810 , GRCh37.p13 chr11: 22,849,356-22,849,356 SVIP, GAS2
    nsv5130860mobile element insertion1nstd203human GRCh38 chr11: 22,828,721-22,828,721 , GRCh37.p13 chr11: 22,850,267-22,850,267 SVIP, GAS2
    nsv5128525mobile element insertion1nstd203human GRCh38 chr11: 22,827,801-22,827,815 , GRCh37.p13 chr11: 22,849,347-22,849,361 SVIP, GAS2
    nsv5120468mobile element insertion1nstd203human GRCh38 chr11: 22,827,811-22,827,811 , GRCh37.p13 chr11: 22,849,357-22,849,357 SVIP, GAS2
    nsv4984285copy number variation1nstd200human GRCh38 chr11: 22,813,734-23,250,368 , GRCh37.p13 chr11: 22,835,280-23,271,914 , GAS2, 3 more genes
    nsv4984261copy number variation1nstd200human GRCh38 chr11: 21,039,520-23,716,274 , GRCh37.p13 chr11: 21,061,066-23,737,820 , WIZP1, 21 more genes
    nsv4978638copy number variation1nstd200human GRCh38 chr11: 22,815,864-22,815,979 , GRCh37.p13 chr11: 22,837,410-22,837,525 SVIP, GAS2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675538copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,290,214-23,743,998 , GRCh38.p12 chr11: 22,268,668-23,722,452 THAP12P4, GAS2, 13 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4675417copy number variation1nstd102humanLikely benign GRCh37 chr11: 22,835,331-23,275,932 , GRCh38.p12 chr11: 22,813,785-23,254,386 LINC02718, SVIP, 2 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
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