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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973682insertion1nstd209human GRCh38 chr11: 64,706,161-64,706,161 , GRCh37.p13 chr11: 64,473,633-64,473,633 NRXN2
    nsv5921361copy number variation1nstd209human GRCh38 chr11: 64,664,720-64,665,010 , GRCh37.p13 chr11: 64,432,192-64,432,482 NRXN2
    nsv5920254copy number variation1nstd209human GRCh38 chr11: 64,703,748-64,705,619 , GRCh37.p13 chr11: 64,471,220-64,473,091 NRXN2
    nsv5916509copy number variation1nstd209human GRCh38 chr11: 64,615,854-64,615,979 , GRCh37.p13 chr11: 64,383,326-64,383,451 NRXN2
    nsv5863665copy number variation1nstd209human GRCh38 chr11: 64,703,739-64,705,608 , GRCh37.p13 chr11: 64,471,211-64,473,080 NRXN2
    nsv5721054mobile element insertion1nstd211human GRCh38 chr11: 64,712,640-64,712,640 , GRCh37.p13 chr11: 64,480,112-64,480,112 NRXN2
    nsv5652845insertion2nstd207human GRCh38 chr11: 64,706,162-64,706,162 , GRCh37.p13 chr11: 64,473,634-64,473,634 NRXN2
    nsv5650878insertion1nstd207human GRCh38 chr11: 64,617,071-64,617,071 , GRCh37.p13 chr11: 64,384,543-64,384,543 NRXN2
    nsv5554983mobile element insertion1nstd206human GRCh38 chr11: 64,712,620-64,712,640 , GRCh37.p13 chr11: 64,480,092-64,480,112 NRXN2
    nsv5494901copy number variation1nstd206human GRCh38 chr11: 64,702,500-64,713,074 , GRCh37.p13 chr11: 64,469,972-64,480,546 NRXN2
    nsv5494828copy number variation1nstd206human GRCh38 chr11: 64,706,079-64,706,223 , GRCh37.p13 chr11: 64,473,551-64,473,695 NRXN2
    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
    nsv5355285translocation1nstd200human GRCh38 chr11: 64,646,586-64,646,586 , GRCh38 chr17: 8,079,708-8,079,708 , GRCh37.p13 chr11: 64,414,058-64,414,058 , GRCh37.p13 chr17: 7,983,026-7,983,026 ALOX12B, NRXN2, 2 more genes
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5260664copy number variation1nstd204human GRCh37.p13 chr11: 64,363,773-64,544,972 , GRCh38.p13 chr11: 64,596,301-64,777,500 PYGM, SF1, 4 more genes
    nsv5191293mobile element insertion1nstd203human GRCh38 chr11: 64,678,732-64,678,739 , GRCh37.p13 chr11: 64,446,204-64,446,211 NRXN2
    nsv4979802copy number variation1nstd200human GRCh38 chr11: 64,703,751-64,705,620 , GRCh37.p13 chr11: 64,471,223-64,473,092 NRXN2
    nsv4979801copy number variation1nstd200human GRCh38 chr11: 64,680,138-64,683,116 , GRCh37.p13 chr11: 64,447,610-64,450,588 NRXN2
    nsv4979800copy number variation1nstd200human GRCh38 chr11: 64,636,884-64,636,979 , GRCh37.p13 chr11: 64,404,356-64,404,451 NRXN2
    nsv4842922copy number variation1nstd200human GRCh37 chr11: 64,471,222-64,473,092 , GRCh38.p12 chr11: 64,703,750-64,705,620 NRXN2
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