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GTR Home > Tests > Variant Resolution Test for PancNext® (+RNAinsight®)

Overview

Test order codeHelp: 8042-R

Test name

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Variant Resolution Test for PancNext® (+RNAinsight®)

Purpose of the test

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This is a clinical test intended for Help: Diagnosis, Pre-symptomatic

Condition

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How to order

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Order URL Help: http://www.ambrygen.com/clinician/ordering-process

Specimen source

Peripheral (whole) blood

Methodology

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Molecular Genetics
DDeletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
RRNA analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

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Clinical utility

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Not provided

Clinical validity

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Clinical validity depends on specific clinical and family history.

Citations

Not provided

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously, Order code: 5555

Practice guidelines

  • AHRQ, 2013
    Technology Assessment on Genetic Testing or Molecular Pathology Testing of Cancers with Unknown Primary Site to Determine Origin (ARCHIVED)

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.