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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4428615copy number variation1nstd174human GRCh37 chr22: 45,135,778-45,136,348 , GRCh38.p12 chr22: 44,739,898-44,740,468 PRR5-ARHGAP8
    nsv589114copy number variation2nstd54human NCBI36 chr22: 43,514,442-43,514,943 , GRCh37.p13 chr22: 45,135,778-45,136,279 , GRCh38.p12 chr22: 44,739,898-44,740,399 PRR5-ARHGAP8

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