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Items: 1 to 20 of 76

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6912414copy number variation1nstd229human GRCh38 chr11: 6,680,001-6,697,500 , GRCh37.p13 chr11: 6,701,232-6,718,731 RPL21P94, MRPL17
    nsv6909148copy number variation1nstd229human GRCh38 chr11: 6,679,401-6,761,147 , GRCh37.p13 chr11: 6,700,632-6,782,378 GVINP2, GVINP1, 2 more genes
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6903917copy number variation1nstd229human GRCh38 chr11: 6,679,982-6,680,316 , GRCh37.p13 chr11: 6,701,213-6,701,547 MRPL17
    nsv6899514copy number variation1nstd229human GRCh38 chr11: 6,602,704-6,989,609 , GRCh37.p13 chr11: 6,623,934-7,010,840 RRP8, OR2AG1, 19 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6437234copy number variation1nstd223human GRCh38 chr11: 6,602,704-6,989,609 , GRCh37.p13 chr11: 6,623,934-7,010,840 ILK, OR2D2, 19 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6290772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,502,523-7,248,333 , GRCh38.p12 chr11: 6,481,293-7,227,102 GVINP2, OR2AG2, 26 more genes
    nsv6132268copy number variation1nstd213human GRCh37 chr11: 6,320,000-6,880,001 , GRCh38.p12 chr11: 6,298,770-6,858,770 APBB1, TPP1, 22 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
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4575447mobile element insertion1nstd166human GRCh37.p13 chr11: 6,701,102-6,701,102 , GRCh38.p12 chr11: 6,679,871-6,679,871 MRPL17
    nsv4456790copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,607,967-6,796,286 , GRCh38.p12 chr11: 6,586,737-6,775,055 ILK, MRPL17, 8 more genes
    nsv4456235copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,896,551-6,719,852 , GRCh38.p12 chr11: 5,875,321-6,698,621 OR52X1P, LOC112268071, 40 more genes
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