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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5508826copy number variation1nstd206human GRCh38 chr11: 18,856,000-18,870,000 , GRCh37.p13 chr11: 18,877,547-18,891,547 MRGPRX7P, LOC645397
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    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
    nsv5373459translocation1nstd200human GRCh38 chr11: 18,574,727-18,574,727 , GRCh38 chr11: 18,864,590-18,864,590 , GRCh37.p13 chr11: 18,596,274-18,596,274 , GRCh37.p13 chr11: 18,886,137-18,886,137 UEVLD, MRGPRX7P
    nsv5340146translocation1nstd200human GRCh37 chr11: 18,886,137-18,886,137 , GRCh37 chr11: 18,596,274-18,596,274 , GRCh38.p12 chr11: 18,864,590-18,864,590 , GRCh38.p12 chr11: 18,574,727-18,574,727 UEVLD, MRGPRX7P
    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
    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
    nsv3971109insertion1nstd168human GRCh38 chr11: 18,847,359-18,866,558 , GRCh37.p13 chr11: 18,868,906-18,888,105 MRGPRX7P
    nsv3960841copy number variation1nstd168human GRCh38 chr11: 18,836,971-18,964,613 , GRCh37.p13 chr11: 18,858,518-18,986,160 MRGPRX1, MRGPRX6P, 5 more genes
    nsv3921634copy number variation1nstd102humanUncertain significance NCBI36 chr11: 18,504,345-20,726,247 , GRCh38 chr11: 18,526,222-20,748,125 , GRCh37 chr11: 18,547,769-20,769,671 NELL1, UEVLD, 41 more genes
    nsv3919437copy number variation1nstd102humanPathogenic GRCh37 chr11: 17,926,636-19,696,051 , NCBI36 chr11: 17,883,212-19,652,627 , GRCh38 chr11: 17,905,089-19,674,505 CSRP3-AS1, ZDHHC13, 55 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
    nsv3901577copy number variation1nstd102humanPathogenic GRCh37 chr11: 18,536,224-31,923,308 , GRCh38.p12 chr11: 18,514,677-31,901,762 LOC105376588, LOC105376585, 137 more genes
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