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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093918copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641 PAFAH1B2, FXYD2, 26 more genes
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7077669inversion1nstd229human GRCh38 chr11: 117,124,022-117,203,209 , GRCh37.p13 chr11: 116,994,738-117,073,925 TAGLN, LOC100652768, 5 more genes
    nsv7061395inversion1nstd229human GRCh38 chr11: 117,060,518-117,209,896 , GRCh37.p13 chr11: 116,931,234-117,080,612 TAGLN, LOC100652768, 6 more genes
    nsv6910993copy number variation1nstd229human GRCh38 chr11: 117,199,432-117,203,001 , GRCh37.p13 chr11: 117,070,148-117,073,717 TAGLN, LOC100652768, 1 more genes
    nsv6910347copy number variation1nstd229human GRCh38 chr11: 117,201,309-117,203,884 , GRCh37.p13 chr11: 117,072,025-117,074,600 LOC100652768, TAGLN, 1 more genes
    nsv6903106copy number variation1nstd229human GRCh38 chr11: 117,172,701-117,691,700 , GRCh37.p13 chr11: 117,043,417-117,562,415 TAGLN, BACE1, 10 more genes
    nsv6900132copy number variation1nstd229human GRCh38 chr11: 117,197,787-117,202,078 , GRCh37.p13 chr11: 117,068,503-117,072,794 PCSK7, SIDT2, 2 more genes
    nsv6594810inversion1nstd223human GRCh38 chr11: 117,134,523-117,210,043 , GRCh37.p13 chr11: 117,005,239-117,080,759 PAFAH1B2, TAGLN, 4 more genes
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 more genes
    nsv6468349copy number variation1nstd223human GRCh38 chr11: 117,207,301-117,210,000 , GRCh37.p13 chr11: 117,078,017-117,080,716 TAGLN, PCSK7
    nsv6461219copy number variation1nstd223human GRCh38 chr11: 117,213,053-117,215,400 , GRCh37.p13 chr11: 117,083,769-117,086,116 PCSK7
    nsv6457366copy number variation1nstd223human GRCh38 chr11: 117,176,601-117,223,100 , GRCh37.p13 chr11: 117,047,317-117,093,816 PAFAH1B2, LOC100652768, 3 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132345copy number variation1nstd213human GRCh37 chr11: 116,860,000-117,080,001 , GRCh38.p12 chr11: 116,989,284-117,209,285 TAGLN, LOC100652768, 8 more genes
    nsv6131835copy number variation1nstd213human GRCh37 chr11: 117,010,000-117,180,001 , GRCh38.p12 chr11: 117,139,284-117,309,285 PAFAH1B2, TAGLN, 7 more genes
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