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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094116copy number variation1nstd102humanPathogenic GRCh37 chr11: 95,523,863-95,564,420 , GRCh38.p12 chr11: 95,790,699-95,831,256 CEP57, MTMR2, 1 more genes
    nsv7093949copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 95,549,619-95,562,458 , GRCh38.p12 chr11: 95,816,455-95,829,294 CEP57
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6906839copy number variation1nstd229human GRCh38 chr11: 95,831,180-95,835,659 , GRCh37.p13 chr11: 95,564,344-95,568,823 MTMR2, CEP57
    nsv6904025copy number variation1nstd229human GRCh38 chr11: 95,797,277-95,797,802 , GRCh37.p13 chr11: 95,530,441-95,530,966 CEP57
    nsv6902781copy number variation1nstd229human GRCh38 chr11: 95,804,688-95,804,851 , GRCh37.p13 chr11: 95,537,852-95,538,015 CEP57
    nsv6900323copy number variation1nstd229human GRCh38 chr11: 93,200,748-96,340,159 , GRCh37.p13 chr11: 92,933,914-96,073,323 FGFR3P2, LOC112268080, 67 more genes
    nsv6899528copy number variation1nstd229human GRCh38 chr11: 95,827,526-95,830,044 , GRCh37.p13 chr11: 95,560,690-95,563,208 CEP57
    nsv6899360copy number variation1nstd229human GRCh38 chr11: 95,791,993-95,795,916 , GRCh37.p13 chr11: 95,525,157-95,529,080 CEP57
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6634412copy number variation1nstd102humanUncertain significance GRCh37 chr11: 94,693,565-95,725,474 , GRCh38.p12 chr11: 94,960,400-95,992,310 SRSF8, LOC105369439, 25 more genes
    nsv6621149copy number variation1nstd224human GRCh37 chr11: 95,565,840-95,621,376 , GRCh38.p12 chr11: 95,832,676-95,888,212 RNA5SP345, MTMR2, 1 more genes
    nsv6582429inversion1nstd223human GRCh38 chr11: 93,899,951-96,855,215 , GRCh37.p13 chr11: 93,633,117-96,726,215 MIR1260B, KDM4E, 51 more genes
    nsv6471730copy number variation1nstd223human GRCh38 chr11: 95,831,183-95,835,658 , GRCh37.p13 chr11: 95,564,347-95,568,822 CEP57, MTMR2
    nsv6462717copy number variation1nstd223human GRCh38 chr11: 95,820,901-95,822,300 , GRCh37.p13 chr11: 95,554,065-95,555,464 CEP57
    nsv6462676copy number variation1nstd223human GRCh38 chr11: 95,832,657-95,833,957 , GRCh37.p13 chr11: 95,565,821-95,567,121 CEP57, MTMR2
    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
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6309455copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,550,941-95,551,077 , GRCh38.p12 chr11: 95,817,777-95,817,913 CEP57
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