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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6917147copy number variation1nstd229human GRCh38 chr11: 59,186,429-59,226,429 , GRCh37.p13 chr11: 58,953,902-58,993,902 MPEG1, RN7SL42P, 1 more genes
    nsv6909854copy number variation1nstd229human GRCh38 chr11: 59,114,527-59,419,074 , GRCh37.p13 chr11: 58,882,000-59,186,547 MPEG1, RN7SL435P, 13 more genes
    nsv6904658copy number variation1nstd229human GRCh38 chr11: 59,209,191-59,214,979 , GRCh37.p13 chr11: 58,976,664-58,982,452 RN7SL42P, MPEG1
    nsv6473550copy number variation1nstd223human GRCh38 chr11: 59,209,190-59,214,978 , GRCh37.p13 chr11: 58,976,663-58,982,451 RN7SL42P, MPEG1
    nsv6470226copy number variation1nstd223human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 LOC105369315, DTX4, 29 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    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
    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
    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
    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
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