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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5908942copy number variation1nstd209human GRCh38 chr11: 61,340,313-61,340,651 , GRCh37.p13 chr11: 61,107,785-61,108,123 TKFC
    nsv5717208mobile element insertion2nstd211human GRCh38 chr11: 61,346,834-61,346,834 , GRCh37.p13 chr11: 61,114,306-61,114,306 TKFC, CYB561A3
    nsv5585747copy number variation1nstd207human GRCh38 chr11: 61,340,313-61,340,651 , GRCh37.p13 chr11: 61,107,785-61,108,123 TKFC
    nsv5500038copy number variation1nstd206human GRCh38 chr11: 61,340,219-61,340,598 , GRCh37.p13 chr11: 61,107,691-61,108,070 TKFC
    nsv5383482mobile element deletion1nstd186human GRCh37 chr11: 61,107,792-61,108,147 , GRCh38.p12 chr11: 61,340,320-61,340,675 TKFC
    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
    nsv5355247translocation1nstd200human GRCh38 chr11: 61,348,409-61,348,409 , GRCh38 chr11: 61,347,854-61,347,854 , GRCh37.p13 chr11: 61,115,326-61,115,326 , GRCh37.p13 chr11: 61,115,881-61,115,881 CYB561A3, TKFC
    nsv5339125translocation1nstd200human GRCh37 chr11: 61,107,800-61,107,800 , GRCh37 chr11: 61,108,062-61,108,062 , GRCh38.p12 chr11: 61,340,590-61,340,590 , GRCh38.p12 chr11: 61,340,328-61,340,328 TKFC
    nsv5326867translocation1nstd204human GRCh38.p13 chr11: 61,340,328-61,340,328 , GRCh38.p13 chr11: 61,340,597-61,340,597 , GRCh37.p13 chr11: 61,108,069-61,108,069 , GRCh37.p13 chr11: 61,107,800-61,107,800 TKFC
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4899679mobile element deletion1nstd200human GRCh38 chr11: 61,340,312-61,340,678 , GRCh37.p13 chr11: 61,107,784-61,108,150 TKFC
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4846499copy number variation1nstd200human GRCh37 chr11: 61,115,326-61,115,881 , GRCh38.p12 chr11: 61,347,854-61,348,409 TKFC, CYB561A3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4745619copy number variation1nstd199human GRCh37 chr11: 61,107,790-61,108,130 , GRCh38.p12 chr11: 61,340,318-61,340,658 TKFC
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4712561copy number variation3nstd195human GRCh37 chr11: 61,107,785-61,107,786 , GRCh38.p12 chr11: 61,340,313-61,340,314 TKFC
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4657495copy number variation1nstd186human GRCh37 chr11: 61,107,800-61,108,124 , GRCh38.p12 chr11: 61,340,328-61,340,652 TKFC
    nsv4648880mobile element deletion1nstd186human GRCh37 chr11: 61,107,786-61,108,124 , GRCh38.p12 chr11: 61,340,314-61,340,652 TKFC
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