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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4578431copy number variation1nstd102humanPathogenic GRCh38 chr9: 136,198,197-136,201,283 , GRCh37 chr9: 139,090,043-139,093,129 LHX3
    nsv3883946copy number variation1nstd102humanPathogenic GRCh38 chr9: 136,197,325-136,205,012 , GRCh37.p13 chr9: 139,089,171-139,096,858 QSOX2, LHX3

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