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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
    nsv6912005copy number variation1nstd229human GRCh38 chr11: 64,878,684-64,901,793 , GRCh37.p13 chr11: 64,646,156-64,669,265 MIR6750, EHD1, 7 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
    nsv6904337copy number variation1nstd229human GRCh38 chr11: 64,888,724-64,889,200 , GRCh37.p13 chr11: 64,656,196-64,656,672 MIR194-2HG, MIR192
    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
    nsv6470306copy number variation1nstd223human GRCh38 chr11: 64,867,530-64,886,506 , GRCh37.p13 chr11: 64,635,002-64,653,978 MIR194-2HG, EHD1, 2 more genes
    nsv6467972copy number variation1nstd223human GRCh38 chr11: 64,845,523-64,919,247 , GRCh37.p13 chr11: 64,612,995-64,686,719 RPS16P6, MIR194-2, 8 more genes
    nsv6466547copy number variation1nstd223human GRCh38 chr11: 64,881,327-64,890,240 , GRCh37.p13 chr11: 64,648,799-64,657,712 RPS16P6, MIR192, 2 more genes
    nsv6463550copy number variation1nstd223human GRCh38 chr11: 64,890,121-64,891,243 , GRCh37.p13 chr11: 64,657,593-64,658,715 MIR194-2HG, MIR192, 1 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
    nsv6189851copy number variation1nstd214human GRCh38 chr11: 64,886,696-64,886,761 , GRCh37.p13 chr11: 64,654,168-64,654,233 MIR194-2HG
    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
    nsv5911506copy number variation1nstd209human GRCh38 chr11: 64,867,547-64,886,490 , GRCh37.p13 chr11: 64,635,019-64,653,962 EHD1, MIR10392, 2 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
    nsv5311501copy number variation1nstd204human GRCh37.p13 chr11: 64,651,307-64,673,688 , GRCh38.p13 chr11: 64,883,835-64,906,216 ATG2A, MIR192, 4 more genes
    nsv5277476copy number variation1nstd204human GRCh38.p13 chr11: 64,883,766-64,893,338 , GRCh37.p13 chr11: 64,651,238-64,660,810 MIR194-2, MIR192, 2 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
    nsv5265385copy number variation1nstd204human GRCh38.p13 chr11: 64,886,505-64,887,789 , GRCh37.p13 chr11: 64,653,977-64,655,261 MIR194-2HG
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