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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922066copy number variation1nstd209human GRCh38 chr11: 32,587,142-32,588,590 , GRCh37.p13 chr11: 32,608,688-32,610,136 EIF3M
    nsv5914601copy number variation1nstd209human GRCh38 chr11: 32,583,926-32,587,007 , GRCh37.p13 chr11: 32,605,472-32,608,553 EIF3M
    nsv5914004copy number variation1nstd209human GRCh38 chr11: 32,589,135-32,589,545 , GRCh37.p13 chr11: 32,610,681-32,611,091 EIF3M
    nsv5908849copy number variation1nstd209human GRCh38 chr11: 32,588,732-32,589,010 , GRCh37.p13 chr11: 32,610,278-32,610,556 EIF3M
    nsv5548643insertion1nstd206human GRCh38 chr11: 32,604,081-32,604,117 , GRCh37.p13 chr11: 32,625,627-32,625,663 CCDC73, EIF3M
    nsv5512757copy number variation1nstd206human GRCh38 chr11: 32,595,013-32,595,965 , GRCh37.p13 chr11: 32,616,559-32,617,511 EIF3M
    nsv5512148copy number variation1nstd206human GRCh38 chr11: 32,600,832-32,601,710 , GRCh37.p13 chr11: 32,622,378-32,623,256 CCDC73, EIF3M
    nsv5501313copy number variation1nstd206human GRCh38 chr11: 32,562,486-32,591,140 , GRCh37.p13 chr11: 32,584,032-32,612,686 EIF3M, HNRNPA3P9
    nsv5498048copy number variation1nstd206human GRCh38 chr11: 32,588,734-32,589,011 , GRCh37.p13 chr11: 32,610,280-32,610,557 EIF3M
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5124377mobile element insertion1nstd203human GRCh38 chr11: 32,604,066-32,604,081 , GRCh37.p13 chr11: 32,625,612-32,625,627 CCDC73, EIF3M
    nsv4986961copy number variation1nstd200human GRCh38 chr11: 32,604,996-32,629,575 , GRCh37.p13 chr11: 32,626,542-32,651,121 EIF3M, CCDC73
    nsv4833684copy number variation1nstd200human GRCh37 chr11: 32,626,535-32,651,120 , GRCh38.p12 chr11: 32,604,989-32,629,574 EIF3M, CCDC73
    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
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4546024insertion1nstd166human GRCh37.p13 chr11: 32,625,612-32,625,612 , GRCh38.p12 chr11: 32,604,066-32,604,066 CCDC73, EIF3M
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 more genes
    nsv4203688copy number variation1nstd166human GRCh37.p13 chr11: 32,622,378-32,623,286 , GRCh38.p12 chr11: 32,600,832-32,601,740 CCDC73, EIF3M
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