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Items: 1 to 20 of 1018

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072383inversion1nstd229human GRCh38 chr11: 100,782,132-100,801,273 , GRCh37.p13 chr11: 100,652,863-100,672,004 ARHGAP42
    nsv7070425inversion1nstd229human GRCh38 chr11: 100,116,010-100,895,806 , GRCh37.p13 chr11: 99,986,742-100,766,537 CNTN5, ARHGAP42, 6 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 more genes
    nsv7062256inversion1nstd229human GRCh38 chr11: 100,833,924-100,834,984 , GRCh37.p13 chr11: 100,704,655-100,705,715 ARHGAP42
    nsv7061741inversion1nstd229human GRCh38 chr11: 100,793,881-105,425,000 , GRCh37.p13 chr11: 100,664,612-105,295,727 MTND1P36, LOC102723862, 75 more genes
    nsv7061479inversion1nstd229human GRCh38 chr11: 100,492,728-100,814,212 , GRCh37.p13 chr11: 100,363,459-100,684,943 ARHGAP42, ARHGAP42-AS1, 2 more genes
    nsv7060803inversion1nstd229human GRCh38 chr11: 100,854,808-101,253,939 , GRCh37.p13 chr11: 100,725,539-101,124,670 PGR, MTMR12P1, 4 more genes
    nsv6917801copy number variation1nstd229human GRCh38 chr11: 100,955,498-100,955,683 , GRCh37.p13 chr11: 100,826,229-100,826,414 ARHGAP42
    nsv6917048copy number variation1nstd229human GRCh38 chr11: 100,875,102-100,875,139 , GRCh37.p13 chr11: 100,745,833-100,745,870 ARHGAP42
    nsv6916600copy number variation1nstd229human GRCh38 chr11: 100,665,261-100,785,688 , GRCh37.p13 chr11: 100,535,992-100,656,419 ARHGAP42, ARHGAP42-AS1, 1 more genes
    nsv6916069copy number variation1nstd229human GRCh38 chr11: 100,617,293-100,756,737 , GRCh37.p13 chr11: 100,488,024-100,627,468 RN7SL222P, ARHGAP42-AS1, 2 more genes
    nsv6915717copy number variation1nstd229human GRCh38 chr11: 100,866,881-100,866,971 , GRCh37.p13 chr11: 100,737,612-100,737,702 ARHGAP42, LOC105369457
    nsv6915009copy number variation1nstd229human GRCh38 chr11: 100,018,339-100,761,990 , GRCh37.p13 chr11: 99,889,071-100,632,721 CNTN5, ARHGAP42, 5 more genes
    nsv6914802copy number variation1nstd229human GRCh38 chr11: 100,753,147-100,755,516 , GRCh37.p13 chr11: 100,623,878-100,626,247 ARHGAP42
    nsv6914764copy number variation1nstd229human GRCh38 chr11: 99,746,178-100,811,774 , GRCh37.p13 chr11: 99,616,909-100,682,505 CNTN5, PPIAP43, 5 more genes
    nsv6914040copy number variation1nstd229human GRCh38 chr11: 100,702,796-100,711,480 , GRCh37.p13 chr11: 100,573,527-100,582,211 ARHGAP42
    nsv6913375copy number variation1nstd229human GRCh38 chr11: 100,844,350-100,845,104 , GRCh37.p13 chr11: 100,715,081-100,715,835 ARHGAP42
    nsv6913033copy number variation1nstd229human GRCh38 chr11: 100,814,153-100,819,619 , GRCh37.p13 chr11: 100,684,884-100,690,350 ARHGAP42
    nsv6913012copy number variation1nstd229human GRCh38 chr11: 100,953,601-100,959,300 , GRCh37.p13 chr11: 100,824,332-100,830,031 ARHGAP42
    nsv6912296copy number variation1nstd229human GRCh38 chr11: 100,690,656-100,693,992 , GRCh37.p13 chr11: 100,561,387-100,564,723 ARHGAP42
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