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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1025381copy number variation1nstd100human NCBI36 chr7: 6,323,229-6,376,343 , GRCh37.p13 chr7: 6,356,704-6,409,818 , GRCh38.p12 chr7: 6,317,073-6,370,187 RPSAP73, FAM220A

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