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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4985045copy number variation1nstd200human GRCh38 chr11: 64,845,523-64,919,251 , GRCh37.p13 chr11: 64,612,995-64,686,723 MIR6750, ATG2A, 8 more genes
    nsv4979811copy number variation1nstd200human GRCh38 chr11: 64,888,295-64,889,293 , GRCh37.p13 chr11: 64,655,767-64,656,765 MIR194-2HG, MIR192
    nsv4834691copy number variation1nstd200human GRCh37 chr11: 64,655,767-64,656,765 , GRCh38.p12 chr11: 64,888,295-64,889,293 MIR192, MIR194-2HG
    nsv4833575copy number variation1nstd200human GRCh37 chr11: 64,651,311-64,673,679 , GRCh38.p12 chr11: 64,883,839-64,906,207 ATG2A, MIR194-2, 4 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
    nsv4607659copy number variation1nstd183human GRCh37 chr11: 64,649,222-64,780,912 , GRCh38.p12 chr11: 64,881,750-65,013,440 MIR6750, MIR6749, 11 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
    nsv4429281copy number variation1nstd174human GRCh37 chr11: 64,655,601-64,684,600 , GRCh38.p12 chr11: 64,888,129-64,917,128 PPP2R5B, ATG2A, 5 more genes
    nsv4210027copy number variation1nstd166human GRCh37.p13 chr11: 64,645,000-64,658,500 , GRCh38.p12 chr11: 64,877,528-64,891,028 EHD1, MIR192, 4 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3902272copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787 ACTN3, GRK2, 157 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
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