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Items: 1 to 20 of 881

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7077976copy number variation1nstd229human GRCh38 chrX: 10,428,917-11,410,756 , GRCh37.p13 chrX: 10,396,957-11,428,876 ARHGAP6, GOT2P7, 5 more genes
    nsv7077714copy number variation1nstd229human GRCh38 chrX: 11,601,066-12,659,464 , GRCh37.p13 chrX: 11,619,186-12,677,583 LIMK2P1, FRMPD4, 5 more genes
    nsv7077547copy number variation1nstd229human GRCh38 chrX: 11,211,476-11,216,212 , GRCh37.p13 chrX: 11,229,596-11,234,332 ARHGAP6
    nsv7077490copy number variation1nstd229human GRCh38 chrX: 11,102,800-11,734,403 , GRCh37.p13 chrX: 11,120,920-11,752,522 HCCS, LOC105373131, 5 more genes
    nsv7077221copy number variation1nstd229human GRCh38 chrX: 10,577,325-11,333,209 , GRCh37.p13 chrX: 10,545,365-11,351,329 ARHGAP6, GOT2P7, 5 more genes
    nsv7076692copy number variation1nstd229human GRCh38 chrX: 11,364,929-11,391,453 , GRCh37.p13 chrX: 11,383,049-11,409,573 ARHGAP6
    nsv7076281copy number variation1nstd229human GRCh38 chrX: 11,387,601-11,388,600 , GRCh37.p13 chrX: 11,405,721-11,406,720 ARHGAP6
    nsv7075611copy number variation1nstd229human GRCh38 chrX: 11,406,306-11,450,715 , GRCh37.p13 chrX: 11,424,426-11,468,835 ARHGAP6
    nsv7075011copy number variation1nstd229human GRCh38 chrX: 11,570,371-11,575,010 , GRCh37.p13 chrX: 11,588,491-11,593,130 ARHGAP6
    nsv7074945copy number variation1nstd229human GRCh38 chrX: 11,072,824-11,273,510 , GRCh37.p13 chrX: 11,090,944-11,291,630 HCCS, ARHGAP6
    nsv7074625copy number variation1nstd229human GRCh38 chrX: 11,461,904-11,467,794 , GRCh37.p13 chrX: 11,480,024-11,485,914 ARHGAP6
    nsv7073622copy number variation1nstd229human GRCh38 chrX: 11,575,273-11,579,613 , GRCh37.p13 chrX: 11,593,393-11,597,733 ARHGAP6
    nsv7073415copy number variation1nstd229human GRCh38 chrX: 11,446,672-11,498,011 , GRCh37.p13 chrX: 11,464,792-11,516,131 ARHGAP6
    nsv7073367copy number variation1nstd229human GRCh38 chrX: 11,270,772-11,382,202 , GRCh37.p13 chrX: 11,288,892-11,400,322 MIR548AX, GOT2P7, 2 more genes
    nsv7073162copy number variation1nstd229human GRCh38 chrX: 11,413,563-11,416,908 , GRCh37.p13 chrX: 11,431,683-11,435,028 ARHGAP6
    nsv7073018copy number variation1nstd229human GRCh38 chrX: 11,264,638-11,264,976 , GRCh37.p13 chrX: 11,282,758-11,283,096 ARHGAP6
    nsv7072609copy number variation1nstd229human GRCh38 chrX: 11,224,588-11,237,430 , GRCh37.p13 chrX: 11,242,708-11,255,550 ARHGAP6
    nsv7072583copy number variation1nstd229human GRCh38 chrX: 11,202,031-11,202,048 , GRCh37.p13 chrX: 11,220,151-11,220,168 ARHGAP6
    nsv7072530copy number variation1nstd229human GRCh38 chrX: 10,726,587-11,190,845 , GRCh37.p13 chrX: 10,694,627-11,208,965 HCCS, ARHGAP6, 1 more genes
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