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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138333copy number variation1nstd232human GRCh37.p13 chr11: 114,397,160-114,397,229 , GRCh38.p12 chr11: 114,526,438-114,526,507 NXPE1, NXPE2
    nsv7076777inversion1nstd229human GRCh38 chr11: 114,180,972-114,778,739 , GRCh37.p13 chr11: 114,051,694-114,649,461 NNMT, NXPE4, 12 more genes
    nsv7064894inversion1nstd229human GRCh38 chr11: 114,542,877-114,618,972 , GRCh37.p13 chr11: 114,413,599-114,489,694 NXPE2, LOC100132172, 2 more genes
    nsv7060444inversion1nstd229human GRCh38 chr11: 114,035,283-115,207,618 , GRCh37.p13 chr11: 113,906,005-115,078,338 CADM1, LOC105369506, 13 more genes
    nsv6913377copy number variation1nstd229human GRCh38 chr11: 114,526,438-114,526,508 , GRCh37.p13 chr11: 114,397,160-114,397,230 NXPE1, NXPE2
    nsv6905472copy number variation1nstd229human GRCh38 chr11: 114,531,850-114,534,941 , GRCh37.p13 chr11: 114,402,572-114,405,663 NXPE2, NXPE1
    nsv6901447copy number variation1nstd229human GRCh38 chr11: 114,532,001-114,548,400 , GRCh37.p13 chr11: 114,402,723-114,419,122 NXPE1, NXPE2
    nsv6898486copy number variation1nstd229human GRCh38 chr11: 114,485,831-114,519,556 , GRCh37.p13 chr11: 114,356,553-114,390,278 NXPE1, NXPE2, 1 more genes
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620884copy number variation1nstd224human GRCh37 chr11: 114,411,343-114,442,145 , GRCh38.p12 chr11: 114,540,621-114,571,423 NXPE4, NXPE1, 1 more genes
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 more genes
    nsv6471861copy number variation1nstd223human GRCh38 chr11: 114,548,601-114,550,600 , GRCh37.p13 chr11: 114,419,323-114,421,322 NXPE1, NXPE2
    nsv6462750copy number variation1nstd223human GRCh38 chr11: 114,530,888-114,735,901 , GRCh37.p13 chr11: 114,401,610-114,606,623 LOC100132172, NXPE2, 2 more genes
    nsv6459663copy number variation1nstd223human GRCh38 chr11: 114,531,601-114,536,000 , GRCh37.p13 chr11: 114,402,323-114,406,722 NXPE2, NXPE1
    nsv6458171copy number variation1nstd223human GRCh38 chr11: 114,490,737-114,538,506 , GRCh37.p13 chr11: 114,361,459-114,409,228 NXPE1, NXPE2, 1 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
    nsv6305232copy number variation1nstd186human GRCh37 chr11: 114,406,817-114,406,872 , GRCh38.p12 chr11: 114,536,095-114,536,150 NXPE2, NXPE1
    nsv6302308copy number variation1nstd186human GRCh37 chr11: 114,414,398-114,414,532 , GRCh38.p12 chr11: 114,543,676-114,543,810 NXPE2, NXPE1
    nsv6294907mobile element insertion1nstd186human GRCh37 chr11: 114,430,634-114,430,685 , GRCh38.p12 chr11: 114,559,912-114,559,963 NXPE1, NXPE2
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
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