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Items: 1 to 20 of 95

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5509825copy number variation1nstd206human GRCh38 chr11: 5,123,827-5,194,475 , GRCh37.p13 chr11: 5,145,057-5,215,705 OR52Z1P, OR52A1, 2 more genes
    nsv5252744copy number variation1nstd204human GRCh38.p13 chr11: 5,127,501-5,131,100 , GRCh37.p13 chr11: 5,148,731-5,152,330 OR52A5
    nsv4977990copy number variation1nstd200human GRCh38 chr11: 5,123,827-5,194,475 , GRCh37.p13 chr11: 5,145,057-5,215,705 OR52A1, OR52Z1P, 2 more genes
    nsv4832719copy number variation1nstd200human GRCh37 chr11: 5,112,289-5,177,946 , GRCh38.p12 chr11: 5,091,059-5,156,716 OR52A5, OR52E3P, 3 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    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
    nsv4729070copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,970,264-5,225,635 , GRCh38.p12 chr11: 4,949,034-5,204,405 OR52A4P, OR52J2P, 16 more genes
    nsv4680228copy number variation1nstd189human GRCh37.p13 chr11: 4,967,265-5,216,022 , GRCh38.p12 chr11: 4,946,035-5,194,792 OR52A1, OR51A1P, 16 more genes
    nsv4675184copy number variation1nstd102humanPathogenic GRCh37 chr11: 5,112,523-5,336,304 , GRCh38.p12 chr11: 5,091,293-5,315,074 OR52A4P, OR52J1P, 16 more genes
    nsv4675058copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,132,252-5,251,954 , GRCh38.p12 chr11: 5,111,022-5,230,724 OR51A1P, OR52A1, 5 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
    nsv4567554mobile element insertion1nstd166human GRCh37.p13 chr11: 5,151,751-5,151,751 , GRCh38.p12 chr11: 5,130,521-5,130,521 OR52A5
    nsv4387795copy number variation1nstd173human GRCh37 chr11: 5,067,391-6,257,231 , GRCh38.p12 chr11: 5,046,161-6,236,001 HBD, OR52N2, 85 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4345375sequence alteration1nstd166human GRCh37.p13 chr11: 5,037,622-5,455,788 , GRCh38.p12 chr11: 5,016,392-5,434,558 HBB, HBE1, 32 more genes
    nsv4209216copy number variation1nstd166human GRCh37.p13 chr11: 4,954,871-5,233,023 , GRCh38.p12 chr11: 4,933,641-5,211,793 OR52J1P, OR51A4, 18 more genes
    nsv4206940copy number variation1nstd166human GRCh37.p13 chr11: 4,980,843-5,188,454 , GRCh38.p12 chr11: 4,959,613-5,167,224 OR52E2, OR52A5, 12 more genes
    nsv4192783copy number variation1nstd166human GRCh37.p13 chr11: 4,640,331-5,290,171 , GRCh38.p12 chr11: 4,619,101-5,268,941 HBE1, OR52E1, 50 more genes
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