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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
    nsv6916754copy number variation1nstd229human GRCh38 chr11: 65,107,601-65,121,800 , GRCh37.p13 chr11: 64,875,073-64,889,272 VPS51, FAU, 3 more genes
    nsv6915986copy number variation1nstd229human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 TM7SF2, HIGD1AP10, 19 more genes
    nsv6914187copy number variation1nstd229human GRCh38 chr11: 65,041,098-65,113,861 , GRCh37.p13 chr11: 64,808,570-64,881,333 TMEM262, TM7SF2, 5 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6470631copy number variation1nstd223human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 MAJIN, HIGD1AP10, 19 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
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 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
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 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
    nsv4679239copy number variation1nstd189human GRCh37.p13 chr11: 64,222,931-65,140,850 , GRCh38.p12 chr11: 64,455,459-65,373,379 ARL2, VPS51, 52 more genes
    nsv4618644copy number variation1nstd183human GRCh37 chr11: 64,883,663-64,889,712 , GRCh38.p12 chr11: 65,116,191-65,122,240 ZNHIT2, FAU, 2 more genes
    nsv4456749copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,396,501-64,883,447 , GRCh38.p12 chr11: 64,629,029-65,115,975 EHD1, TM7SF2, 32 more genes
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 more genes
    nsv4202114copy number variation1nstd166human GRCh37.p13 chr11: 64,876,000-64,903,500 , GRCh38.p12 chr11: 65,108,528-65,136,029 VPS51, MRPL49, 5 more genes
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