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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv6913437copy number variation1nstd229human GRCh38 chr11: 19,627,651-19,793,614 , GRCh37.p13 chr11: 19,649,197-19,815,160 NAV2, LEISA1, 1 more genes
    nsv6912878copy number variation1nstd229human GRCh38 chr11: 19,226,049-19,889,512 , GRCh37.p13 chr11: 19,247,596-19,911,058 MIR4694, NAV2-AS4, 8 more genes
    nsv6911780copy number variation1nstd229human GRCh38 chr11: 19,358,091-20,660,220 , GRCh37.p13 chr11: 19,379,638-20,681,766 RNA5SP335, HMGB1P40, 14 more genes
    nsv6906158copy number variation1nstd229human GRCh38 chr11: 18,831,701-26,837,040 , GRCh37.p13 chr11: 18,853,248-26,858,587 HTATIP2, LINC02686, 68 more genes
    nsv6437818copy number variation1nstd223human GRCh38 chr11: 19,709,745-19,711,327 , GRCh37.p13 chr11: 19,731,291-19,732,873 LEISA1, NAV2
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5863913copy number variation1nstd209human GRCh38 chr11: 19,705,088-19,709,155 , GRCh37.p13 chr11: 19,726,634-19,730,701 LEISA1, NAV2
    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
    nsv4978511copy number variation1nstd200human GRCh38 chr11: 19,709,745-19,711,327 , GRCh37.p13 chr11: 19,731,291-19,732,873 LEISA1, NAV2
    nsv4844965copy number variation1nstd200human GRCh37 chr11: 19,731,291-19,732,873 , GRCh38.p12 chr11: 19,709,745-19,711,327 NAV2, LEISA1
    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
    nsv4486613mobile element insertion1nstd166human GRCh37.p13 chr11: 19,733,462-19,733,462 , GRCh38.p12 chr11: 19,711,916-19,711,916 LEISA1, NAV2
    nsv4212152copy number variation1nstd166human GRCh37.p13 chr11: 19,731,291-19,732,873 , GRCh38.p12 chr11: 19,709,745-19,711,327 NAV2, LEISA1
    nsv4206781copy number variation1nstd166human GRCh37.p13 chr11: 19,729,252-19,730,717 , GRCh38.p12 chr11: 19,707,706-19,709,171 NAV2, LEISA1
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