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Items: 1 to 20 of 91

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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
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6911893copy number variation1nstd229human GRCh38 chr11: 12,979,326-12,985,943 , GRCh37.p13 chr11: 13,000,873-13,007,490 LINC00958
    nsv6908124copy number variation1nstd229human GRCh38 chr11: 12,983,158-13,006,624 , GRCh37.p13 chr11: 13,004,705-13,028,171 RASSF10-DT, LINC00958
    nsv6905351copy number variation1nstd229human GRCh38 chr11: 12,978,698-12,978,882 , GRCh37.p13 chr11: 13,000,245-13,000,429 LINC00958
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6443797copy number variation1nstd223human GRCh38 chr11: 12,978,727-12,979,026 , GRCh37.p13 chr11: 13,000,274-13,000,573 LINC00958
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5909845copy number variation1nstd209human GRCh38 chr11: 12,975,167-12,985,716 , GRCh37.p13 chr11: 12,996,714-13,007,263 LINC00958
    nsv5852317copy number variation1nstd209human GRCh38 chr11: 12,976,037-12,985,455 , GRCh37.p13 chr11: 12,997,584-13,007,002 LINC00958
    nsv5713176mobile element insertion1nstd211human GRCh38 chr11: 12,982,927-12,982,927 , GRCh37.p13 chr11: 13,004,474-13,004,474 LINC00958
    nsv5506056copy number variation1nstd206human GRCh38 chr11: 12,989,329-12,989,412 , GRCh37.p13 chr11: 13,010,876-13,010,959 LINC00958
    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
    nsv4978298copy number variation1nstd200human GRCh38 chr11: 12,989,329-12,989,412 , GRCh37.p13 chr11: 13,010,876-13,010,959 LINC00958
    nsv4978297copy number variation1nstd200human GRCh38 chr11: 12,983,158-13,006,622 , GRCh37.p13 chr11: 13,004,705-13,028,169 LINC00958, RASSF10-DT
    nsv4978296copy number variation1nstd200human GRCh38 chr11: 12,981,515-12,981,587 , GRCh37.p13 chr11: 13,003,062-13,003,134 LINC00958
    nsv4842173copy number variation1nstd200human GRCh37 chr11: 13,000,274-13,000,573 , GRCh38.p12 chr11: 12,978,727-12,979,026 LINC00958
    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
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