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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4424493copy number variation1nstd174human GRCh37 chr22: 45,135,829-45,137,741 , GRCh38.p12 chr22: 44,739,949-44,741,861 PRR5-ARHGAP8
    nsv589120copy number variation1nstd54human NCBI36 chr22: 43,514,829-43,516,405 , GRCh37.p13 chr22: 45,136,165-45,137,741 , GRCh38.p12 chr22: 44,740,285-44,741,861 PRR5-ARHGAP8

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