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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6905371copy number variation1nstd229human GRCh38 chr11: 7,803,252-8,125,113 , GRCh37.p13 chr11: 7,824,799-8,146,660 OR5P3, EIF3F, 12 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5127061mobile element insertion1nstd203human GRCh38 chr11: 8,009,738-8,009,785 , GRCh37.p13 chr11: 8,031,285-8,031,332 CASC23
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 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
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4565647inversion1nstd166human GRCh37.p13 chr11: 6,776,274-9,026,287 , GRCh38.p12 chr11: 6,755,043-9,004,740 , ZNF215, 61 more genes
    nsv4456276copy number variation1nstd102humanUncertain significance GRCh37 chr11: 7,953,436-8,303,138 , GRCh38.p12 chr11: 7,931,889-8,281,591 OR10A3, LOC105376536, 9 more genes
    nsv4370152copy number variation1nstd173human GRCh37 chr11: 6,629,042-8,085,652 , GRCh38.p12 chr11: 6,607,812-8,064,105 LOC105376533, GVINP2, 48 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4201399copy number variation1nstd166human GRCh37.p13 chr11: 8,032,155-8,032,516 , GRCh38.p12 chr11: 8,010,608-8,010,969 CASC23
    nsv3923443copy number variation1nstd102humanUncertain significance NCBI36 chr11: 7,973,799-10,415,328 , GRCh37 chr11: 8,017,223-10,458,752 , GRCh38 chr11: 7,995,676-10,437,205 TMEM41B, AKIP1, 51 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
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