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Items: 1 to 20 of 141

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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
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6910589copy number variation1nstd229human GRCh38 chr11: 10,598,193-10,611,741 , GRCh37.p13 chr11: 10,619,740-10,633,288 IRAG1-AS1, IRAG1
    nsv6900630copy number variation1nstd229human GRCh38 chr11: 10,558,245-10,558,706 , GRCh37.p13 chr11: 10,579,792-10,580,253 IRAG1-AS1, LYVE1
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6450885copy number variation1nstd223human GRCh38 chr11: 10,539,801-10,544,400 , GRCh37.p13 chr11: 10,561,348-10,565,947 IRAG1-AS1, RNF141
    nsv6439816copy number variation1nstd223human GRCh38 chr11: 10,586,782-10,586,793 , GRCh37.p13 chr11: 10,608,329-10,608,340 IRAG1-AS1, IRAG1
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6099628insertion1nstd212human GRCh38 chr11: 10,539,699-10,539,699 , GRCh37.p13 chr11: 10,561,246-10,561,246 IRAG1-AS1, RNF141
    nsv6031522copy number variation1nstd212human GRCh38 chr11: 10,585,559-10,585,643 , GRCh37.p13 chr11: 10,607,106-10,607,190 IRAG1, IRAG1-AS1
    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
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