We offer the Variantyx Unity™ whole genome sequencing (WGS) test for diagnosis of rare inherited disorders. Patient samples are processed via our Genomic Intelligence® platform, using provided phenotype information to guide the analysis. Our board-certified medical geneticists consult with the ordering clinician or genetic counselor to review the analysis results and generate a signed clinical report.
|Price2||Turn Around Time
|Variantyx Unity™ WGS1 Singleton (CPT codes: 81229, 81415, see FAQ)||$2,819||6-8|
|Variantyx Unity™ WGS1 Trio (CPT codes: 81229, 81415, 81416 x2, see FAQ)||$5,597||6-8|
1WGS analysis includes small sequence change, gross structural variant (CNV), short tandem repeat and mitochondrial genome sequencing analysis. Conducted on Illumina platform using Illumina TruSeq DNA PCR-Free Library Preparation Kit at 30X mean mappable coverage.
2Pricing is for institutional billing and direct patient payment options.
Insurance billing is available, with eligibility determined through a benefits investigation process (see FAQ). Payment by institutional billing or direct patient payment is also accepted. Orders are subject to accepting test requisition and informed consent forms. Local taxes may apply.
To place an order, please fill out the form below. After your order is received, one of our clinical coordinators will get in touch to obtain information needed to initiate benefits investigation, to provide the informed consent and requisition forms and to coordinate sample collection and shipping. For help in placing an order, please contact our clinical coordinators directly at firstname.lastname@example.org.