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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4414348copy number variation1nstd174human GRCh37 chr14: 67,058,780-67,140,282 , GRCh38.p12 chr14: 66,592,062-66,673,564 GPHN
    nsv1051980copy number variation1nstd100human NCBI36 chr14: 66,145,759-66,210,035 , GRCh37.p13 chr14: 67,076,006-67,140,282 , GRCh38.p12 chr14: 66,609,288-66,673,564 GPHN

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