We dedicate ourselves to providing you accessible, affordable, and high-quality lab services.

HNL Genomics (CTGT) , a department of HNL Lab Medicine, contracts with the insurance providers listed here. We highly recommend however that our patients contact their insurance provider to verify coverage and laboratory benefits – especially if you are a new patient of HNL Genomics (CTGT) .  If your insurance plan is not listed here, please contact your insurer to verify your laboratory benefit. 

Please be aware that benefits and coverage change regularly, and that some plans require use of a specific laboratory.  If you are in a self-funded insurance plan, please check with your employer to verify laboratory benefits.

    Aetna (Some plans require PCP selection)
    AmeriHealth Caritas Pennsylvania
    AmeriHealth Caritas VIP
    Beech Street
    Blue Choice
    Capital Blue Cross/Capital Advantage Plans
    Blue Journey HMO/PPO/Alliance
    InterGroup Services (IGS)
    Blue Ridge Health Network
    Keystone 65 (**)
    Health Care Solutions Corp. (HCSC)
    Cigna EPO Plans
    Independence Blue Cross
    Cigna HMO
    Keystone Health Plan Central
    Cigna Indemnity Plans
    Medical Assistance – New Jersey
    Cigna PPO Health Plans
    Consolidated Health Plan
    Coventry Health Care
    EHP Significa
    EHP, Inc.
    Federal Black Lung
    Federal Employees Compensation Act
    Gateway (**)
    Geisinger Health Plans
    Great West Health Plans
    Health America/Health Assurance
    Health Care Solutions Corp. (HCSC)
    Highmark Blue Shield Plans
    Humana Medicare PFFS Products
    IHP-Integrated Health Plan
    Magellan Behavioral Health Plan
    Medical Assistance - Pennsylvania
    National Preferred Provider Network (NPPN)
    PA Health & Wellness
    Personal Choice
    Prime Health Services
    Private Health Care Systems (PHCS)
    Spectrum Administrators (with the exception of Eastern PA Health Network‹ EPHN›)
    TriCare Humana Military
    • Choice / Choice Plus Plans
    • Navigate Plans
    • OneNet PPO
    • Veteran’s Affairs (VACCN)
    UPMC Health Plans
    Valley Preferred
    Vibra Health Plans
    WellCare Medicare Advantage PFFS

HNL Genomics (CTGT) , a department of HNL Lab Medicine, participates with 50+ major insurance company plans and over 300 plan types. We dedicate ourselves to providing you accessible, affordable, and high-quality lab services. If your insurance is not listed, please contact a HNL Genomics (CTGT) billing expert at 844-HNL-BILL (toll-free) for verification of HNL Lab Medicine participation or contact your insurance company directly.

The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. HNL Lab Medicine strongly recommends confirmation of CPT codes with third-party payors and/or the AMA. We assume no responsibility for billing errors due to reliance upon CPT codes provided by HNL Lab Medicine.


October 28, 2022

Non-Hodgkin Lymphoma FISH Panel Now Available

B-cell lymphoma is a large group of heterogenous disorders and comprises a majority of non-Hodgkin lymphomas.
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October 20, 2022

Genetic testing for Familial Transthyretin Amyloidosis (TTR) NOW AVAILABLE In-House

Hereditary amyloidosis is a life-threatening disorder that can lead to peripheral neuropathy and heart failure.
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August 08, 2022

Familial hypercholesterolemia (FH)

Familial hypercholesterolemia (FH) is a genetic disorder that increases the likelihood of having coronary heart disease at a younger age. Learn about how to determine if you have hypercholesterolemia and what actions you can take to create better outcomes!

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April 11, 2022

Genome Sequencing: A Vital Tool Used in Identifying and Tracking New COVID-19 Variants

Genome sequencing is reading or decoding the complete genetic information i.e. “Genome” of an organism that is encrypted in the form of a very long string called DNA made up of 4 letters, A, T, G, and C. The genome of an organism essentially determines their physical characteristics and ...
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March 03, 2022

The Effect of Genetics on Individual Heart Health: Early Identification of FH Variations to Optimize Treatment

Test must be ordered by a Physician.

Familial hypercholesterolemia (FH) is a genetic disorder that is characterized by abnormally high blood levels of low-density lipoprotein (LDL) cholesterol, sometimes referred to as "bad cholesterol". This condition affects an estimated 1 in 250 people, and increases the likelihood of developing cardiovascular disease. In fact, FH is estimated to be the cause of 2-3% of heart attacks in individuals younger than age 60.

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