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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
    nsv5268235copy number variation1nstd204human GRCh38.p13 chr11: 62,664,401-62,843,200 , GRCh37.p13 chr11: 62,431,873-62,610,672 HNRNPUL2, UQCC3, 23 more genes
    nsv5121368mobile element insertion1nstd203human GRCh38 chr11: 62,788,069-62,788,083 , GRCh37.p13 chr11: 62,555,541-62,555,555 TMEM223, TMEM179B, 1 more genes
    nsv4985021copy number variation1nstd200human GRCh38 chr11: 62,788,505-62,793,926 , GRCh37.p13 chr11: 62,555,977-62,561,398 TMEM179B, TMEM223, 3 more genes
    nsv4979719copy number variation1nstd200human GRCh38 chr11: 62,789,064-62,791,541 , GRCh37.p13 chr11: 62,556,536-62,559,013 TMEM179B, TMEM223, 3 more genes
    nsv4848009copy number variation1nstd200human GRCh37 chr11: 62,555,977-62,561,398 , GRCh38.p12 chr11: 62,788,505-62,793,926 MIR6514, MIR6748, 3 more genes
    nsv4831520copy number variation1nstd200human GRCh37 chr11: 62,556,536-62,559,013 , GRCh38.p12 chr11: 62,789,064-62,791,541 MIR6748, NXF1, 3 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
    nsv4613749copy number variation1nstd183human GRCh37 chr11: 62,336,160-62,568,472 , GRCh38.p12 chr11: 62,568,688-62,801,000 LRRN4CL, HNRNPUL2-BSCL2, 26 more genes
    nsv4495984mobile element insertion1nstd166human GRCh37.p13 chr11: 62,555,541-62,555,541 , GRCh38.p12 chr11: 62,788,069-62,788,069 TMEM223, TMEM179B, 1 more genes
    nsv4456974copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,487,052-62,788,240 , GRCh38.p12 chr11: 62,719,580-63,020,768 RN7SL259P, SNORD29, 29 more genes
    nsv4455787copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,314,663-62,788,240 , GRCh38.p12 chr11: 62,547,191-63,020,768 TTC9C, POLR2G, 48 more genes
    nsv4209873copy number variation1nstd166human GRCh37.p13 chr11: 62,555,974-62,559,348 , GRCh38.p12 chr11: 62,788,502-62,791,876 TMEM223, TMEM179B, 3 more genes
    nsv4203700copy number variation1nstd166human GRCh37.p13 chr11: 62,555,555-62,555,894 , GRCh38.p12 chr11: 62,788,083-62,788,422 TMEM223, TMEM179B, 1 more genes
    nsv3922416copy number variation1nstd102humanPathogenic GRCh38 chr11: 62,433,886-63,096,003 , NCBI36 chr11: 61,957,934-62,620,051 , GRCh37 chr11: 62,201,358-62,863,475 TAF6L, TMEM179B, 51 more genes
    nsv3913554copy number variation1nstd102humanPathogenic NCBI36 chr11: 61,976,619-62,386,829 , GRCh37 chr11: 62,220,043-62,630,253 , GRCh38 chr11: 62,452,571-62,862,781 NXF1, SNORA57, 43 more genes
    nsv3912559copy number variation1nstd102humanPathogenic GRCh38 chr11: 62,249,520-62,946,093 , GRCh37 chr11: 62,016,992-62,713,565 , NCBI36 chr11: 61,773,568-62,470,141 SNORD28, SCGB1A1, 53 more genes
    nsv3911700copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,330,308-62,608,042 , GRCh38 chr11: 62,562,836-62,840,570 , NCBI36 chr11: 62,086,884-62,364,618 TAF6L, CSKMT, 32 more genes
    nsv3909634copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 61,840,997-62,987,330 , GRCh38.p12 chr11: 62,073,525-63,219,858 CHRM1, EEF1G, 66 more genes
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