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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978402insertion1nstd209human GRCh38 chr11: 10,539,699-10,539,699 , GRCh37.p13 chr11: 10,561,246-10,561,246 RNF141, IRAG1-AS1
    nsv5512178copy number variation1nstd206human GRCh38 chr11: 10,545,495-10,545,609 , GRCh37.p13 chr11: 10,567,042-10,567,156 IRAG1-AS1
    nsv5503111copy number variation1nstd206human GRCh38 chr11: 10,587,078-10,590,455 , GRCh37.p13 chr11: 10,608,625-10,612,002 IRAG1, IRAG1-AS1
    nsv4984197copy number variation1nstd200human GRCh38 chr11: 10,587,078-10,590,455 , GRCh37.p13 chr11: 10,608,625-10,612,002 IRAG1-AS1, IRAG1
    nsv4984196copy number variation1nstd200human GRCh38 chr11: 10,564,193-10,564,566 , GRCh37.p13 chr11: 10,585,740-10,586,113 LYVE1, IRAG1-AS1
    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
    nsv4731536copy number variation1nstd199human GRCh37 chr11: 10,607,081-10,607,160 , GRCh38.p12 chr11: 10,585,534-10,585,613 IRAG1-AS1, IRAG1
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4367321copy number variation1nstd173human GRCh37 chr11: 9,422,923-11,175,143 , GRCh38.p12 chr11: 9,401,376-11,153,596 , LOC107984309, 40 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
    nsv4211399copy number variation1nstd166human GRCh37.p13 chr11: 10,601,544-10,607,785 , GRCh38.p12 chr11: 10,579,997-10,586,238 IRAG1-AS1, IRAG1
    nsv4202266copy number variation1nstd166human GRCh37.p13 chr11: 10,585,740-10,586,113 , GRCh38.p12 chr11: 10,564,193-10,564,566 IRAG1-AS1, LYVE1
    nsv3947082insertion1nstd167human GRCh37 chr11: 10,561,238-10,561,238 , GRCh38.p12 chr11: 10,539,691-10,539,691 RNF141, IRAG1-AS1
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3915585copy number variation1nstd102humanPathogenic NCBI36 chr11: 9,967,639-16,803,929 , GRCh37 chr11: 10,011,063-16,847,353 , GRCh38 chr11: 9,989,516-16,825,806 BTBD10, LOC107984370, 86 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
    nsv3912175copy number variation1nstd102humanPathogenic NCBI36 chr11: 10,107,142-14,047,625 , GRCh37.p13 chr11: 10,150,566-14,091,049 , GRCh38.p12 chr11: 10,129,019-14,069,502 LINC02545, CENPUP1, 58 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
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