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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967811insertion1nstd209human GRCh38 chr11: 86,056,134-86,056,134 , GRCh37.p13 chr11: 85,767,176-85,767,176 PICALM
    nsv5920899copy number variation1nstd209human GRCh38 chr11: 85,426,274-86,526,514 , GRCh37.p13 chr11: 85,137,318-86,237,556 SYTL2, ME3, 23 more genes
    nsv5719952mobile element insertion1nstd211human GRCh38 chr11: 86,063,398-86,063,398 , GRCh37.p13 chr11: 85,774,440-85,774,440 PICALM
    nsv5707748mobile element insertion2nstd211human GRCh38 chr11: 86,008,949-86,008,949 , GRCh37.p13 chr11: 85,719,992-85,719,992 PICALM
    nsv5706013mobile element insertion1nstd211human GRCh38 chr11: 85,970,184-85,970,184 , GRCh37.p13 chr11: 85,681,227-85,681,227 PICALM
    nsv5704461mobile element insertion1nstd211human GRCh38 chr11: 86,063,334-86,063,334 , GRCh37.p13 chr11: 85,774,376-85,774,376 PICALM
    nsv5698983mobile element insertion2nstd211human GRCh38 chr11: 86,033,428-86,033,428 , GRCh37.p13 chr11: 85,744,470-85,744,470 PICALM
    nsv5509546copy number variation1nstd206human GRCh38 chr11: 85,982,085-85,986,783 , GRCh37.p13 chr11: 85,693,128-85,697,826 PICALM
    nsv5505850copy number variation1nstd206human GRCh38 chr11: 86,047,034-87,555,409 , GRCh37.p13 chr11: 85,758,076-87,266,301 , OR7E2P, 32 more genes
    nsv5504409copy number variation1nstd206human GRCh38 chr11: 86,047,944-86,050,000 , GRCh37.p13 chr11: 85,758,986-85,761,042 PICALM
    nsv5503592copy number variation1nstd206human GRCh38 chr11: 86,033,407-86,033,550 , GRCh37.p13 chr11: 85,744,449-85,744,592 PICALM
    nsv5499146copy number variation1nstd206human GRCh38 chr11: 86,045,952-86,046,910 , GRCh37.p13 chr11: 85,756,994-85,757,952 PICALM
    nsv5413885mobile element insertion1nstd206human GRCh38 chr11: 86,033,428-86,033,479 , GRCh37.p13 chr11: 85,744,470-85,744,521 PICALM
    nsv5402352mobile element insertion1nstd206human GRCh38 chr11: 85,970,184-85,970,235 , GRCh37.p13 chr11: 85,681,227-85,681,278 PICALM
    nsv5400045mobile element insertion1nstd206human GRCh38 chr11: 86,063,334-86,063,385 , GRCh37.p13 chr11: 85,774,376-85,774,427 PICALM
    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
    nsv5319128copy number variation1nstd204human GRCh38.p13 chr11: 85,976,805-86,081,423 , GRCh37.p13 chr11: 85,687,848-85,792,465 PICALM
    nsv5278686copy number variation1nstd204human GRCh38.p13 chr11: 86,052,262-86,059,962 , GRCh37.p13 chr11: 85,763,304-85,771,004 PICALM
    nsv5274177copy number variation1nstd204human GRCh38.p13 chr11: 85,976,601-86,081,600 , GRCh37.p13 chr11: 85,687,644-85,792,642 PICALM
    nsv5271719copy number variation1nstd204human GRCh38.p13 chr11: 85,983,381-85,984,480 , GRCh37.p13 chr11: 85,694,424-85,695,523 PICALM
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