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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093841copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,418,390-19,204,313 , GRCh38.p12 chr11: 18,396,843-19,182,766 UEVLD, ZDHHC13, 25 more genes
    nsv7070173inversion1nstd229human GRCh38 chr11: 18,169,244-18,915,403 , GRCh37.p13 chr11: 18,190,791-18,936,950 TSG101, MIR3159, 33 more genes
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv6914375copy number variation1nstd229human GRCh38 chr11: 18,769,656-18,793,452 , GRCh37.p13 chr11: 18,791,203-18,814,999 PTPN5
    nsv6908987copy number variation1nstd229human GRCh38 chr11: 18,767,599-18,774,906 , GRCh37.p13 chr11: 18,789,146-18,796,453 PTPN5
    nsv6904937copy number variation1nstd229human GRCh38 chr11: 18,771,515-18,772,284 , GRCh37.p13 chr11: 18,793,062-18,793,831 PTPN5
    nsv6902561copy number variation1nstd229human GRCh38 chr11: 18,728,701-18,732,800 , GRCh37.p13 chr11: 18,750,248-18,754,347 PTPN5
    nsv6902148copy number variation1nstd229human GRCh38 chr11: 18,723,761-18,726,437 , GRCh37.p13 chr11: 18,745,308-18,747,984 IGSF22, PTPN5
    nsv6901931copy number variation1nstd229human GRCh38 chr11: 18,665,485-18,742,365 , GRCh37.p13 chr11: 18,687,032-18,763,912 SRSF3P1, IGSF22, 2 more genes
    nsv6637654copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,784,556-18,797,650 , GRCh38.p12 chr11: 17,763,009-18,776,103 LOC112268073, SAAL1, 37 more genes
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 more genes
    nsv6452316copy number variation1nstd223human GRCh38 chr11: 18,755,730-18,756,647 , GRCh37.p13 chr11: 18,777,277-18,778,194 PTPN5
    nsv6442874copy number variation1nstd223human GRCh38 chr11: 18,725,544-18,727,002 , GRCh37.p13 chr11: 18,747,091-18,748,549 PTPN5, IGSF22
    nsv6437295copy number variation1nstd223human GRCh38 chr11: 18,767,599-18,774,900 , GRCh37.p13 chr11: 18,789,146-18,796,447 PTPN5
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6314200copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,482,438-18,792,764 , GRCh38.p12 chr11: 18,460,891-18,771,217 LDHAL6A, SPTY2D1, 11 more genes
    nsv6247825mobile element insertion1nstd215human GRCh38 chr11: 18,746,170-18,746,170 , GRCh37.p13 chr11: 18,767,717-18,767,717 PTPN5
    nsv6132357copy number variation1nstd213human GRCh37 chr11: 18,780,000-19,070,001 , GRCh38.p12 chr11: 18,758,453-19,048,454 MRGPRX1, MRGPRX5P, 8 more genes
    nsv5909130copy number variation1nstd209human GRCh38 chr11: 18,752,036-18,752,124 , GRCh37.p13 chr11: 18,773,583-18,773,671 PTPN5
    nsv5512699copy number variation1nstd206human GRCh38 chr11: 18,746,486-18,747,398 , GRCh37.p13 chr11: 18,768,033-18,768,945 PTPN5
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