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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
    nsv7069673inversion1nstd229human GRCh38 chr11: 19,148,674-19,583,004 , GRCh37.p13 chr11: 19,170,221-19,604,551 RNA5SP335, CSRP3, 8 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
    nsv6911840copy number variation1nstd229human GRCh38 chr11: 19,207,516-19,227,827 , GRCh37.p13 chr11: 19,229,063-19,249,374 E2F8, CSRP3-AS1
    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
    nsv6620907copy number variation1nstd224human GRCh37 chr11: 19,234,797-19,247,287 , GRCh38.p12 chr11: 19,213,250-19,225,740 CSRP3-AS1, E2F8
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 more genes
    nsv6581264inversion1nstd223human GRCh38 chr11: 19,233,533-19,233,991 , GRCh37.p13 chr11: 19,255,080-19,255,538 CSRP3-AS1, E2F8
    nsv6451422copy number variation1nstd223human GRCh38 chr11: 19,207,516-19,227,827 , GRCh37.p13 chr11: 19,229,063-19,249,374 CSRP3-AS1, E2F8
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6294756mobile element insertion1nstd186human GRCh37 chr11: 19,260,677-19,260,728 , GRCh38.p12 chr11: 19,239,130-19,239,181 E2F8, CSRP3-AS1
    nsv6247828mobile element insertion1nstd215human GRCh38 chr11: 19,232,851-19,232,851 , GRCh37.p13 chr11: 19,254,398-19,254,398 CSRP3-AS1, E2F8
    nsv5710242mobile element insertion2nstd211human GRCh38 chr11: 19,239,130-19,239,130 , GRCh37.p13 chr11: 19,260,677-19,260,677 E2F8, CSRP3-AS1
    nsv5694649mobile element insertion2nstd211human GRCh38 chr11: 19,227,529-19,227,529 , GRCh37.p13 chr11: 19,249,076-19,249,076 CSRP3-AS1, E2F8
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5409721mobile element insertion1nstd206human GRCh38 chr11: 19,239,130-19,239,181 , GRCh37.p13 chr11: 19,260,677-19,260,728 CSRP3-AS1, E2F8
    nsv5399672mobile element insertion1nstd206human GRCh38 chr11: 19,227,529-19,227,580 , GRCh37.p13 chr11: 19,249,076-19,249,127 CSRP3-AS1, E2F8
    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
    nsv5317297copy number variation1nstd204human GRCh38.p13 chr11: 18,870,874-19,367,180 , GRCh37.p13 chr11: 18,892,421-19,388,727 PCNAP4, CSRP3, 12 more genes
    nsv5259610copy number variation1nstd204human GRCh38.p13 chr11: 19,197,938-19,225,475 , GRCh37.p13 chr11: 19,219,485-19,247,022 E2F8, CSRP3-AS1, 1 more genes
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