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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6905925copy number variation1nstd229human GRCh38 chr11: 95,752,466-95,757,673 , GRCh37.p13 chr11: 95,485,630-95,490,837 FGFR3P2
    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
    nsv6900221copy number variation1nstd229human GRCh38 chr11: 95,755,201-95,761,700 , GRCh37.p13 chr11: 95,488,365-95,494,864 FGFR3P2
    nsv6898949copy number variation1nstd229human GRCh38 chr11: 95,757,286-95,758,622 , GRCh37.p13 chr11: 95,490,450-95,491,786 FGFR3P2
    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
    nsv6582429inversion1nstd223human GRCh38 chr11: 93,899,951-96,855,215 , GRCh37.p13 chr11: 93,633,117-96,726,215 MIR1260B, KDM4E, 51 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
    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
    nsv6302338copy number variation1nstd186human GRCh37 chr11: 95,490,449-95,491,785 , GRCh38.p12 chr11: 95,757,285-95,758,621 FGFR3P2
    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
    nsv6132294copy number variation1nstd213human GRCh37 chr11: 95,460,000-96,160,001 , GRCh38.p12 chr11: 95,726,836-96,426,837 RNA5SP345, RPL32P25, 8 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5507999copy number variation1nstd206human GRCh38 chr11: 95,757,285-95,758,621 , GRCh37.p13 chr11: 95,490,449-95,491,785 FGFR3P2
    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
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4971755copy number variation1nstd200human GRCh38 chr11: 95,757,285-95,758,621 , GRCh37.p13 chr11: 95,490,449-95,491,785 FGFR3P2
    nsv4208685copy number variation1nstd166human GRCh37.p13 chr11: 95,490,449-95,491,785 , GRCh38.p12 chr11: 95,757,285-95,758,621 FGFR3P2
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