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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5695451mobile element insertion1nstd211human GRCh38 chr11: 60,298,164-60,298,164 , GRCh37.p13 chr11: 60,065,637-60,065,637 MS4A4A
    nsv5498810copy number variation1nstd206human GRCh38 chr11: 60,275,074-60,281,074 , GRCh37.p13 chr11: 60,042,547-60,048,547 MS4A4A
    nsv5399455mobile element insertion1nstd206human GRCh38 chr11: 60,298,164-60,298,215 , GRCh37.p13 chr11: 60,065,637-60,065,688 MS4A4A
    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
    nsv5373651translocation1nstd200human GRCh38 chr11: 60,280,776-60,280,776 , GRCh38 chr11: 60,181,876-60,181,876 , GRCh37.p13 chr11: 59,949,349-59,949,349 , GRCh37.p13 chr11: 60,048,249-60,048,249 MS4A6A, MS4A4A
    nsv5342493translocation1nstd200human GRCh37 chr11: 59,949,349-59,949,349 , GRCh37 chr11: 60,048,249-60,048,249 , GRCh38.p12 chr11: 60,181,876-60,181,876 , GRCh38.p12 chr11: 60,280,776-60,280,776 MS4A4A, MS4A6A
    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
    nsv5304784copy number variation1nstd204human GRCh37.p13 chr11: 60,004,311-60,071,559 , GRCh38.p13 chr11: 60,236,838-60,304,086 MS4A4E, MS4A4A
    nsv5271945copy number variation1nstd204human GRCh38.p13 chr11: 60,296,471-60,297,670 , GRCh37.p13 chr11: 60,063,944-60,065,143 MS4A4A
    nsv5261383copy number variation1nstd204human GRCh38.p13 chr11: 60,236,891-60,283,961 , GRCh37.p13 chr11: 60,004,364-60,051,434 MS4A4E, MS4A4A
    nsv5139256mobile element insertion1nstd203human GRCh38 chr11: 60,286,799-60,286,814 , GRCh37.p13 chr11: 60,054,272-60,054,287 MS4A4A
    nsv5124797mobile element insertion1nstd203human GRCh38 chr11: 60,296,172-60,296,188 , GRCh37.p13 chr11: 60,063,645-60,063,661 MS4A4A
    nsv4979615copy number variation1nstd200human GRCh38 chr11: 60,302,415-60,313,545 , GRCh37.p13 chr11: 60,069,888-60,081,018 MS4A4A
    nsv4979614copy number variation1nstd200human GRCh38 chr11: 60,300,918-60,302,017 , GRCh37.p13 chr11: 60,068,391-60,069,490 MS4A4A
    nsv4979612copy number variation1nstd200human GRCh38 chr11: 60,236,845-60,304,077 , GRCh37.p13 chr11: 60,004,318-60,071,550 MS4A4E, MS4A4A
    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
    nsv4840658copy number variation1nstd200human GRCh37 chr11: 60,004,318-60,071,550 , GRCh38.p12 chr11: 60,236,845-60,304,077 MS4A4A, MS4A4E
    nsv4838915copy number variation1nstd200human GRCh37 chr11: 60,068,391-60,069,490 , GRCh38.p12 chr11: 60,300,918-60,302,017 MS4A4A
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