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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
    nsv6914042copy number variation1nstd229human GRCh38 chr11: 59,190,448-59,208,573 , GRCh37.p13 chr11: 58,957,921-58,976,046 MPEG1, DTX4
    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
    nsv6904323copy number variation1nstd229human GRCh38 chr11: 58,827,321-59,212,101 , GRCh37.p13 chr11: 58,594,794-58,979,574 LOC100422399, LOC105369315, 14 more genes
    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
    nsv6080900insertion1nstd212human GRCh38 chr11: 59,209,875-59,209,875 , GRCh37.p13 chr11: 58,977,348-58,977,348 MPEG1
    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
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