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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093772copy number variation1nstd102humanPathogenic GRCh37 chr11: 61,197,619-61,552,680 , GRCh38.p12 chr11: 61,430,147-61,785,208 LOC105369331, CPSF7, 12 more genes
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6917433copy number variation1nstd229human GRCh38 chr11: 61,472,401-62,010,600 , GRCh37.p13 chr11: 61,239,873-61,778,072 LOC105369329, FADS3, 24 more genes
    nsv6912721copy number variation1nstd229human GRCh38 chr11: 61,782,988-61,783,092 , GRCh37.p13 chr11: 61,550,460-61,550,564 MYRF
    nsv6909200copy number variation1nstd229human GRCh38 chr11: 61,458,001-62,069,400 , GRCh37.p13 chr11: 61,225,473-61,836,872 RPS2P37, BEST1, 25 more genes
    nsv6905915copy number variation1nstd229human GRCh38 chr11: 61,787,251-61,820,694 , GRCh37.p13 chr11: 61,554,723-61,588,166 FADS2, MYRF, 5 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6905487copy number variation1nstd229human GRCh38 chr11: 61,782,334-61,782,377 , GRCh37.p13 chr11: 61,549,806-61,549,849 MYRF
    nsv6904042copy number variation1nstd229human GRCh38 chr11: 61,456,701-62,012,000 , GRCh37.p13 chr11: 61,224,173-61,779,472 LOC399900, LRRC10B, 24 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    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
    nsv6039720copy number variation1nstd212human GRCh38 chr11: 61,760,024-61,760,090 , GRCh37.p13 chr11: 61,527,496-61,527,562 MYRF
    nsv5925773copy number variation1nstd209human GRCh38 chr11: 61,752,371-61,752,421 , GRCh37.p13 chr11: 61,519,843-61,519,893 MYRF, MYRF-AS1
    nsv5507750copy number variation1nstd206human GRCh38 chr11: 61,788,760-61,788,908 , GRCh37.p13 chr11: 61,556,232-61,556,380 MYRF, TMEM258
    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
    nsv4979658copy number variation1nstd200human GRCh38 chr11: 61,771,377-61,771,457 , GRCh37.p13 chr11: 61,538,849-61,538,929 MYRF
    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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
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