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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112724copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 117,278,620-117,284,002 , GRCh38.p12 chr11: 117,407,904-117,413,286 CEP164
    nsv5972868insertion1nstd209human GRCh38 chr11: 117,357,726-117,357,726 , GRCh37.p13 chr11: 117,228,442-117,228,442 CEP164
    nsv5910161copy number variation1nstd209human GRCh38 chr11: 117,357,130-117,357,453 , GRCh37.p13 chr11: 117,227,846-117,228,169 CEP164
    nsv5726770mobile element insertion2nstd211human GRCh38 chr11: 117,357,738-117,357,738 , GRCh37.p13 chr11: 117,228,454-117,228,454 CEP164
    nsv5724513mobile element insertion2nstd211human GRCh38 chr11: 117,324,502-117,324,502 , GRCh37.p13 chr11: 117,195,218-117,195,218 CEP164
    nsv5712951mobile element insertion1nstd211human GRCh38 chr11: 117,369,718-117,369,718 , GRCh37.p13 chr11: 117,240,434-117,240,434 CEP164
    nsv5648261insertion1nstd207human GRCh38 chr11: 117,324,484-117,324,484 , GRCh37.p13 chr11: 117,195,200-117,195,200 CEP164
    nsv5595747copy number variation1nstd207human GRCh38 chr11: 117,320,376-117,320,533 , GRCh37.p13 chr11: 117,191,092-117,191,249 CEP164
    nsv5558250mobile element insertion1nstd206human GRCh38 chr11: 117,324,502-117,324,553 , GRCh37.p13 chr11: 117,195,218-117,195,269 CEP164
    nsv5541071insertion1nstd206human GRCh38 chr11: 117,369,718-117,369,736 , GRCh37.p13 chr11: 117,240,434-117,240,452 CEP164
    nsv5513899copy number variation1nstd206human GRCh38 chr11: 117,394,480-117,394,929 , GRCh37.p13 chr11: 117,265,196-117,265,645 CEP164
    nsv5513562copy number variation1nstd206human GRCh38 chr11: 117,310,673-117,329,839 , GRCh37.p13 chr11: 117,181,389-117,200,555 CEP164, BACE1
    nsv5512514copy number variation1nstd206human GRCh38 chr11: 117,325,678-117,326,484 , GRCh37.p13 chr11: 117,196,394-117,197,200 CEP164
    nsv5509071copy number variation1nstd206human GRCh38 chr11: 117,354,892-117,359,371 , GRCh37.p13 chr11: 117,225,608-117,230,087 CEP164
    nsv5508510copy number variation1nstd206human GRCh38 chr11: 117,325,028-117,356,143 , GRCh37.p13 chr11: 117,195,744-117,226,859 PRR13P3, CEP164
    nsv5502057copy number variation1nstd206human GRCh38 chr11: 117,346,480-117,351,225 , GRCh37.p13 chr11: 117,217,196-117,221,941 CEP164
    nsv5499578copy number variation1nstd206human GRCh38 chr11: 117,404,104-117,412,628 , GRCh37.p13 chr11: 117,274,820-117,283,344 CEP164
    nsv5493920copy number variation1nstd206human GRCh38 chr11: 117,320,346-117,320,918 , GRCh37.p13 chr11: 117,191,062-117,191,634 CEP164
    nsv5380882copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-117,222,724 , GRCh38.p12 chr11: 117,338,587-117,352,008 CEP164
    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
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