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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5710013mobile element insertion1nstd211human GRCh38 chr11: 59,209,109-59,209,109 , GRCh37.p13 chr11: 58,976,582-58,976,582 MPEG1
    nsv5645246insertion1nstd207human GRCh38 chr11: 59,209,875-59,209,875 , GRCh37.p13 chr11: 58,977,348-58,977,348 MPEG1
    nsv5404871mobile element insertion1nstd206human GRCh38 chr11: 59,209,109-59,209,160 , GRCh37.p13 chr11: 58,976,582-58,976,633 MPEG1
    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
    nsv5373650translocation1nstd200human GRCh38 chr11: 59,209,244-59,209,244 , GRCh38 chr11: 59,285,724-59,285,724 , GRCh37.p13 chr11: 59,053,197-59,053,197 , GRCh37.p13 chr11: 58,976,717-58,976,717 LOC643709, MPEG1
    nsv5326104inversion1nstd204human GRCh37.p13 chr11: 58,446,123-60,252,987 , GRCh38.p13 chr11: 58,678,650-60,485,514 OSBP, OR5BB1P, 78 more genes
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984973copy number variation1nstd200human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 GLYATL1P4, LOC283194, 29 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4870911inversion1nstd200human GRCh37 chr11: 58,446,132-60,252,987 , GRCh38.p12 chr11: 58,678,659-60,485,514 LOC100422398, LOC100287485, 78 more genes
    nsv4759073insertion1nstd199human GRCh37 chr11: 58,977,359-58,977,359 , GRCh38.p12 chr11: 59,209,886-59,209,886 MPEG1
    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
    nsv4729406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 58,602,498-59,091,934 , GRCh38.p12 chr11: 58,835,025-59,324,461 LOC100422398, LOC643709, 20 more genes
    nsv4486969mobile element insertion1nstd166human GRCh37.p13 chr11: 58,976,569-58,976,569 , GRCh38.p12 chr11: 59,209,096-59,209,096 MPEG1
    nsv4446141insertion1nstd175human GRCh37 chr11: 58,977,348-58,977,348 , GRCh38.p12 chr11: 59,209,875-59,209,875 MPEG1
    nsv4207944copy number variation1nstd166human GRCh37.p13 chr11: 58,975,169-59,051,729 , GRCh38.p12 chr11: 59,207,696-59,284,256 MPEG1, WARS1P1, 3 more genes
    nsv4196768copy number variation1nstd166human GRCh37.p13 chr11: 58,979,183-59,055,905 , GRCh38.p12 chr11: 59,211,710-59,288,432 MPEG1, WARS1P1, 3 more genes
    nsv3949853insertion1nstd167human GRCh37 chr11: 58,977,372-58,977,372 , GRCh38.p12 chr11: 59,209,899-59,209,899 MPEG1
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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