Skip to content
Contact Us Portal Login
Variantyx
  • 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
        • Cardiomyopathy and Arrhythmia Analysis
        • DMD Analysis
        • Endocrinology Analysis
        • Hearing Loss Disorders Analysis
        • Nephrology Disorders Analysis
        • Pediatric Hematologic Disorders Analysis
        • Retinal Disorders Analysis
      • Hereditary Cancer
        • Comprehensive Hereditary Cancer Analysis
        • Common Hereditary Cancer Analysis
        • Hereditary Hematologic Cancer 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
        • Ataxia Repeat Expansion Analysis
        • Comprehensive Ataxia Analysis
        • Dementia Analysis
        • Epilepsy Analysis
        • Motor Neuron Disorders Analysis
        • Movement Disorders Analysis
        • Muscular Dystrophy Analysis
        • DMD Analysis
        • Neuromuscular Disorders Analysis
        • Neuropathies Analysis
        • X-linked Intellectual Disability Plus Analysis
    • Rapid Genome
      • Neonatal
      • Pediatric
      • Standard
    • Reproductive Genetics
      • CNV Analysis
      • Comprehensive Analysis
    • Precision Oncology
      • Hereditary Cancer
        • Comprehensive Hereditary Cancer Analysis
        • Common Hereditary Cancer Analysis
        • Hereditary Hematologic Cancer 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
      • FAQs
    • Ask Your Doctor
      • About Prenatal Genetic Testing
      • About Ataxia Testing
      • About CMT Testing
      • About Epilepsy Testing
      • About Mitochondrial Disorders Testing
    • Tell Us Your Story
  • Providers
    • The Variantyx Difference
    • Billing Information
    • Specimen Requirements
    • FAQs
    • Rare Genetic Disorders
    • Reproductive Genetics
    • 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
      • FAQs
    • 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
      • FAQs
      • Webinars
    • Case Studies
      • Missed By Others
      • First-Line Testing
      • Dual Diagnosis
    • Webinars
    • Publications
    • Licenses
  • Company
    • About Us
    • Join Our Team!
    • News Center
    • Mission & Values
    • Contact Us

Saliva Sample Collection Instructions

Saliva Swab Collection Instructions
Assisted Saliva Swab Collection Instructions
Saliva Collection Instructions

ORAcollect.Dx (OCD-100/OCD-100A) collection instructions

Oragene.DNA OG-575 format (assisted collection kit) user instructions

Oragene.DNA collection instructions (OG-600/610/500/510)

Need more information?

Contact us
Variantyx © 2026 Variantyx, Inc. All rights reserved
  • Licenses
  • Website Privacy Policy
  • Contact Us
  • Terms of Use
  • Site Map
  • 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
        • Cardiomyopathy and Arrhythmia Analysis
        • DMD Analysis
        • Endocrinology Analysis
        • Hearing Loss Disorders Analysis
        • Nephrology Disorders Analysis
        • Pediatric Hematologic Disorders Analysis
        • Retinal Disorders Analysis
      • Hereditary Cancer
        • Comprehensive Hereditary Cancer Analysis
        • Common Hereditary Cancer Analysis
        • Hereditary Hematologic Cancer 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
        • Ataxia Repeat Expansion Analysis
        • Comprehensive Ataxia Analysis
        • Dementia Analysis
        • Epilepsy Analysis
        • Motor Neuron Disorders Analysis
        • Movement Disorders Analysis
        • Muscular Dystrophy Analysis
        • DMD Analysis
        • Neuromuscular Disorders Analysis
        • Neuropathies Analysis
        • X-linked Intellectual Disability Plus Analysis
    • Rapid Genome
      • Neonatal
      • Pediatric
      • Standard
    • Reproductive Genetics
      • CNV Analysis
      • Comprehensive Analysis
    • Precision Oncology
      • Hereditary Cancer
        • Comprehensive Hereditary Cancer Analysis
        • Common Hereditary Cancer Analysis
        • Hereditary Hematologic Cancer 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
      • FAQs
    • Ask Your Doctor
      • About Prenatal Genetic Testing
      • About Ataxia Testing
      • About CMT Testing
      • About Epilepsy Testing
      • About Mitochondrial Disorders Testing
    • Tell Us Your Story
  • Providers
    • The Variantyx Difference
    • Billing Information
    • Specimen Requirements
    • FAQs
    • Rare Genetic Disorders
    • Reproductive Genetics
    • 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
      • FAQs
    • 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
      • FAQs
      • Webinars
    • Case Studies
      • Missed By Others
      • First-Line Testing
      • Dual Diagnosis
    • Webinars
    • Publications
    • Licenses
  • Company
    • About Us
    • Join Our Team!
    • News Center
    • Mission & Values
    • Contact Us
Contact Us
Portal Login
Upcoming Talk | Thursday, Mar 12, 2026 @11:20am | ACMG Exhibit Theater 1
Upcoming Talk Thursday, Mar 12, 2026 @11:20am ACMG Exhibit Theater 1

Join Christine Stanley, PhD, FACMG as she presents The Long and Short of It: How Long and Short-Read Genome Sequencing Uncovers Elusive Diagnoses.

background image

Join Christine Stanley, PhD, FACMG as she presents The Long and Short of It: How Long and Short-Read Genome Sequencing Uncovers Elusive Diagnoses.

JOIN US AT ACMG