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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684084copy number variation1nstd102humanAffects GRCh38 chr2: 126,690,252-126,690,308 , GRCh37 chr2: 127,447,828-127,447,884 GYPC
    nsv7137197copy number variation2nstd102humanPathogenic, Affects GRCh38 chr16: 72,054,504-72,076,977 , GRCh37.p13 chr16: 72,088,403-72,110,876 TXNL4B, HP, 1 more genes

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