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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv526029copy number variation1nstd21human NCBI35 chr2: 132,567,013-133,185,147 , GRCh37.p13 chr2: 132,733,281-133,351,415 , GRCh38.p12 chr2: 131,975,708-132,593,842 GPR39, FAM201B, 17 more genes

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