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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314476translocation1nstd102humanUncertain significance GRCh37 chr7: 81,106,821-81,106,821 , GRCh38.p12 chr7: 81,477,505-81,477,505 , GRCh38.p12 chr4: 120,216,282-120,216,282 , GRCh37 chr4: 121,137,437-121,137,437 , GRCh38.p12 chr4|NT_187544.1: 52,099-52,099 0

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