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GTR Home > Tests > Familial Variant Targeted Sequencing

How to order

Test Order CodeHelp: FMLIS

How To Order

Laboratory's Test Page

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https://www.nationwidechildrens.org/specialties/laboratory-services

How To Order

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Samples can be accepted 7 days a week (Monday - Sunday). All samples must be labeled with minimum of two patient identifying information (e.g. Patient Name and Date of Birth). Please submit all samples with a completed test requisition form.
Order URL Help: https://www.nationwidechildrens.org/specialties/laboratory-services

Informed Consent Required Help: No

Specimen Source

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  • Amniotic fluid
  • Cord blood
  • Cystic hygroma fluid
  • Fetal blood
  • Fresh tissue
  • Frozen tissue
  • Isolated DNA
  • Peripheral (whole) blood
  • Product of conception (POC)
  • Saliva
  • Skin

Specimen requirements: https://www.nationwidechildrens.org/specialties/laboratory-services

Test Codes

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CPT© Code(s):
81403

Other test codes on lab website

Test Orderable By

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  • Genetic Counselor
  • Health Care Provider
  • Licensed Physician
  • Nurse Practitioner

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Maternal cell contamination study (MCC), comments
  • Tissue Culture, Order code: TCULT, comments
  • Custom Prenatal Testing
  • Custom mutation-specific/Carrier testing

Ordering Requirements

Genetic Counseling Required Pre-test Help
No
Genetic Counseling Required Post-test Help
No

Contact Policy

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  • Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.

CPT only. Copyright 2012 American Medical Association. All rights reserved.

  • Click here for the notice regarding AMA CPT codes.

Clinical resources

Practice guidelines

  • ACMG, 2016
    Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
  • ASHG/ACMG, 2015
    Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents
  • ACMG, 2015
    Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics.
  • ACMG, 2015
    Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
  • ACMG, 2013
    ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.