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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6916226copy number variation1nstd229human GRCh38 chr11: 115,388,630-115,407,663 , GRCh37.p13 chr11: 115,259,348-115,278,381 CADM1, CADM1-AS1
    nsv6915589copy number variation1nstd229human GRCh38 chr11: 115,390,973-115,455,059 , GRCh37.p13 chr11: 115,261,691-115,325,778 CADM1-AS1, CADM1
    nsv6914024copy number variation1nstd229human GRCh38 chr11: 115,318,107-115,416,737 , GRCh37.p13 chr11: 115,188,826-115,287,455 CADM1-AS1, CADM1, 1 more genes
    nsv6909398copy number variation1nstd229human GRCh38 chr11: 115,343,831-115,409,486 , GRCh37.p13 chr11: 115,214,550-115,280,204 CADM1, CADM1-AS1
    nsv6909296copy number variation1nstd229human GRCh38 chr11: 115,390,418-115,462,131 , GRCh37.p13 chr11: 115,261,136-115,332,850 CADM1, CADM1-AS1
    nsv6903486copy number variation1nstd229human GRCh38 chr11: 115,380,215-115,446,445 , GRCh37.p13 chr11: 115,250,933-115,317,164 CADM1, CADM1-AS1
    nsv6901787copy number variation1nstd229human GRCh38 chr11: 114,713,382-115,839,694 , GRCh37.p13 chr11: 114,584,104-115,710,412 LINC02698, LOC105369506, 10 more genes
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 more genes
    nsv6470716copy number variation1nstd223human GRCh38 chr11: 115,390,417-115,462,130 , GRCh37.p13 chr11: 115,261,135-115,332,849 CADM1, CADM1-AS1
    nsv6465013copy number variation1nstd223human GRCh38 chr11: 115,318,101-115,416,700 , GRCh37.p13 chr11: 115,188,820-115,287,418 CADM1-AS1, CADM1, 1 more genes
    nsv6458539copy number variation1nstd223human GRCh38 chr11: 115,388,630-115,407,662 , GRCh37.p13 chr11: 115,259,348-115,278,380 CADM1-AS1, CADM1
    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
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv5978212inversion1nstd209human GRCh37.p13 chr11: 115,262,143-115,319,508 , GRCh38 chr11: 115,391,425-115,448,789 CADM1, CADM1-AS1
    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
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4980800copy number variation1nstd200human GRCh38 chr11: 115,390,417-115,462,130 , GRCh37.p13 chr11: 115,261,135-115,332,849 CADM1, CADM1-AS1
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