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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112718copy number variation1nstd102humanUncertain significance GRCh38 chr11: 32,963,226-33,107,103 , GRCh37.p13 chr11: 32,984,772-33,128,649 DEPDC7, PIGCP1, 5 more genes
    nsv5849906copy number variation1nstd209human GRCh38 chr11: 32,960,411-32,961,810 , GRCh37.p13 chr11: 32,981,957-32,983,356 QSER1, LOC105376615
    nsv5714017mobile element insertion1nstd211human GRCh38 chr11: 32,905,781-32,905,781 , GRCh37.p13 chr11: 32,927,327-32,927,327 QSER1
    nsv5705242mobile element insertion2nstd211human GRCh38 chr11: 32,902,402-32,902,402 , GRCh37.p13 chr11: 32,923,948-32,923,948 QSER1
    nsv5698513mobile element insertion1nstd211human GRCh38 chr11: 32,916,251-32,916,251 , GRCh37.p13 chr11: 32,937,797-32,937,797 QSER1
    nsv5651992insertion1nstd207human GRCh38 chr11: 32,916,238-32,916,238 , GRCh37.p13 chr11: 32,937,784-32,937,784 QSER1
    nsv5552378insertion1nstd206human GRCh38 chr11: 32,925,639-32,925,775 , GRCh37.p13 chr11: 32,947,185-32,947,321 QSER1
    nsv5539057insertion1nstd206human GRCh38 chr11: 32,916,251-32,916,289 , GRCh37.p13 chr11: 32,937,797-32,937,835 QSER1
    nsv5511241copy number variation1nstd206human GRCh38 chr11: 32,903,458-32,904,232 , GRCh37.p13 chr11: 32,925,004-32,925,778 QSER1
    nsv5510899copy number variation1nstd206human GRCh38 chr11: 32,970,559-32,972,629 , GRCh37.p13 chr11: 32,992,105-32,994,175 QSER1, LOC105376615
    nsv5498612copy number variation1nstd206human GRCh38 chr11: 32,754,246-32,927,890 , GRCh37.p13 chr11: 32,775,792-32,949,436 , RPL34P2, 3 more genes
    nsv5495531copy number variation1nstd206human GRCh38 chr11: 32,917,622-32,917,790 , GRCh37.p13 chr11: 32,939,168-32,939,336 QSER1
    nsv5406363mobile element insertion1nstd206human GRCh38 chr11: 32,902,402-32,902,453 , GRCh37.p13 chr11: 32,923,948-32,923,999 QSER1
    nsv5405871mobile element insertion1nstd206human GRCh38 chr11: 32,905,781-32,905,832 , GRCh37.p13 chr11: 32,927,327-32,927,378 QSER1
    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
    nsv5354914translocation1nstd200human GRCh38 chr11: 32,903,482-32,903,482 , GRCh38 chr11: 32,904,212-32,904,212 , GRCh37.p13 chr11: 32,925,758-32,925,758 , GRCh37.p13 chr11: 32,925,028-32,925,028 QSER1
    nsv5331432translocation1nstd200human GRCh37 chr11: 32,990,866-32,990,866 , GRCh37 chr11: 32,990,945-32,990,945 , GRCh38.p12 chr11: 32,969,399-32,969,399 , GRCh38.p12 chr11: 32,969,320-32,969,320 LOC105376615, QSER1
    nsv5301776copy number variation1nstd204human GRCh38.p13 chr11: 32,903,457-32,904,241 , GRCh37.p13 chr11: 32,925,003-32,925,787 QSER1
    nsv5131860mobile element insertion1nstd203human GRCh38 chr11: 32,916,238-32,916,251 , GRCh37.p13 chr11: 32,937,784-32,937,797 QSER1
    nsv5127746mobile element insertion1nstd203human GRCh38 chr11: 32,916,240-32,916,251 , GRCh37.p13 chr11: 32,937,786-32,937,797 QSER1
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