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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4685729copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,401,423-97,401,593 , GRCh38.p12 chr9: 94,639,141-94,639,311 FBP1
    nsv4683559copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,401,403-97,401,612 , GRCh38.p12 chr9: 94,639,121-94,639,330 FBP1

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