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      • Exome Analysis
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        • Genome-Wide CNV and FMR1 Analysis
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  • Our Tests
    • Rare Genetic Disorders
      • Genomic Unity® 2.0
      • Whole Genome Analysis
      • Exome Plus Analysis
      • Exome Analysis
      • CNV Analyses
        • Constitutional Genome-Wide Copy Number Variant Analysis
        • Genome-Wide CNV and FMR1 Analysis
      • Mitochondrial Disorders
        • Mitochondrial Genome Sequence Analysis
        • Mitochondrial Genome Deletions Analysis
        • Nuclear Encoded Mitochondrial Gene Analysis
        • Comprehensive Mitochondrial Disorders Analysis
      • Other Targeted Analyses
        • Renal Disorders Analysis
        • Retinal Disorders Analysis
        • Hearing Loss Disorders Analysis
        • Endocrinology Analysis
      • Hereditary Cancer
        • Comprehensive Hereditary Cancer Analysis
        • Common Hereditary Cancer Analysis
        • Colorectal Cancer Analysis
        • BRCA1/2 Analysis
      • Custom Analysis
    • Neurology Analyses
      • Genomic Unity® 2.0
      • Whole Genome Analysis
      • Exome Plus Analysis
      • Exome Analysis
      • CNV Analyses
        • Constitutional Genome-Wide Copy Number Variant Analysis
        • Genome-Wide CNV and FMR1 Analysis
      • Targeted Analyses
        • Epilepsy Analysis
        • Motor Neuron Disorders Analysis
        • Movement Disorders Analysis
        • Comprehensive Ataxia Analysis
        • Ataxia Repeat Expansion Analysis
        • Neuromuscular Disorders Analysis
        • Muscular Dystrophy Analysis
        • Neuropathies Analysis
        • Dementia Analysis
        • X-linked Intellectual Disability Plus Analysis
    • Rapid Genome (NICU/PICU)
      • Lightning Genome Analysis
    • Reproductive Genetics – IriSight™
      • CNV Analysis
      • Prenatal Analysis
      • Pregnancy Loss Analysis
    • Precision Oncology
      • Somatic Analysis
        • Solid Tumor Analysis
      • Hereditary Cancer
        • Comprehensive Hereditary Cancer Analysis
        • Common Hereditary Cancer Analysis
        • Colorectal Cancer Analysis
        • BRCA1/2 Analysis
    • Custom Analysis
    • Wellness
      • Genomic Inform®
  • Patients
    • The Variantyx Difference
    • Billing Information
    • Rare Genetic Disorders
    • Reproductive Genetics
    • Wellness Testing
    • Patient Resources
      • How to Get Your Results
      • Doctor Discussion Guides
      • Patient Advocacy Resources
      • How to Collect and Send a Sample
      • FAQ
    • Tell Us Your Story
  • Providers
    • The Variantyx Difference
    • Billing Information
    • Specimen Requirements
    • FAQs
    • Rare Genetic Disorders
    • Reproductive Genetics
    • Precision Oncology
    • Wellness Testing
    • Provider Resources
      • Testing Forms
      • Working Together
      • Repeat Expansions Analyzed
      • ACMG Secondary and Other Actionable (Incidental) Findings
        • List of Secondary Findings Genes
      • Understanding Variantyx Reports
      • Testing Customized for Your Institution
      • Webinars
  • Resources
    • Patient Resources
      • How to Get Your Results
      • Billing Information
      • Doctor Discussion Guides
      • Patient Advocacy Resources
      • How to Collect and Send a Sample
      • FAQ
    • Provider Resources
      • Testing Forms
      • Billing Information
      • Working Together
      • Repeat Expansions Analyzed
      • ACMG Secondary and Other Actionable (Incidental) Findings
      • List of Secondary Findings Genes
      • Understanding Variantyx Reports
      • Specimen Requirements
      • Testing Customized for Your Institution
      • FAQ
      • Webinars
    • Case Studies
    • Licenses
  • Company
    • About Us
    • Join Our Team!
    • News Center
    • Mission & Values
    • Contact Us
  • Connect With Us
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