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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5505357copy number variation1nstd206human GRCh38 chr11: 18,884,283-18,886,720 , GRCh37.p13 chr11: 18,905,830-18,908,267 MRGPRX6P
    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
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv5317297copy number variation1nstd204human GRCh38.p13 chr11: 18,870,874-19,367,180 , GRCh37.p13 chr11: 18,892,421-19,388,727 PCNAP4, CSRP3, 12 more genes
    nsv5255430copy number variation1nstd204human GRCh38.p13 chr11: 18,870,501-19,367,200 , GRCh37.p13 chr11: 18,892,048-19,388,747 MRGPRX10P, MRGPRX11P, 12 more genes
    nsv5241169copy number variation1nstd204human GRCh38.p13 chr11: 18,870,176-18,903,448 , GRCh37.p13 chr11: 18,891,723-18,924,995 LOC645397, MRGPRX6P
    nsv4984246copy number variation1nstd200human GRCh38 chr11: 18,870,877-19,367,171 , GRCh37.p13 chr11: 18,892,424-19,388,718 MRGPRX2, MRGPRX9P, 12 more genes
    nsv4978486copy number variation1nstd200human GRCh38 chr11: 18,887,875-18,889,363 , GRCh37.p13 chr11: 18,909,422-18,910,910 MRGPRX6P
    nsv4978485copy number variation1nstd200human GRCh38 chr11: 18,884,283-18,886,720 , GRCh37.p13 chr11: 18,905,830-18,908,267 MRGPRX6P
    nsv4848235copy number variation1nstd200human GRCh37 chr11: 18,892,424-19,388,718 , GRCh38.p12 chr11: 18,870,877-19,367,171 LOC645397, MRGPRX10P, 12 more genes
    nsv4834770copy number variation1nstd200human GRCh37 chr11: 18,905,830-18,908,267 , GRCh38.p12 chr11: 18,884,283-18,886,720 MRGPRX6P
    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
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4456526copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,894,624-19,554,521 , GRCh38.p12 chr11: 18,873,077-19,532,974 MRGPRX11P, NAV2, 15 more genes
    nsv4369688copy number variation1nstd173human GRCh37 chr11: 18,894,625-18,930,933 , GRCh38.p12 chr11: 18,873,078-18,909,386 LOC645397, MRGPRX6P, 1 more genes
    nsv4208761copy number variation1nstd166human GRCh37.p13 chr11: 18,133,425-18,936,070 , GRCh38.p12 chr11: 18,111,878-18,914,523 , UEVLD, 37 more genes
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