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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1397901copy number variation1nstd45humanPathogenic GRCh38.p12 chr6: 50,818,726-50,847,613 , GRCh37 chr6: 50,786,439-50,815,326 TFAP2B

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