HNL Genomics

About Our Tests

Our HNL Genomic division offers a comprehensive test menu for genetic testing that covers a variety of genetic disorders. 

Genomics Test Directory

Genomic Expertise You can Count on

HNL Genomics offers the highest standards for quality and accuracy, ensuring reliable results. With quick turnaround times, an extensive panel selection, and access to a diverse range of expertise, you can count on us to find answers to the most difficult questions. 

HNL Genomics Specialties

HNL Genomics is committed to providing excellent, timely results for oncology providers and patients.

Get the answers you need quickly and accurately with a team dedicated to comprehensive oncology testing. We utilize innovative methods and technologies to perform cost-effective tests with excellent turnaround times.

Develop personalized treatment plans for your patients through results you can trust. Our expanded NGS solid tumor panel analyzes 500+ genes, with results in as little as 14 days. The extensive cytogenetics FISH panel covers overs 50 FISH assays for neoplastic diseases with 3-5 days of turn around time. Contact our team of genetic experts today. 

Frequently Ordered Oncology Tests

Visit the Genomics Test Directory to learn more about the tests we offer.

Genomics Test Directory

The HNL Genomics group is proud to offer an ever-expanding menu to meet the needs of your cardiology patients.

Whether you are testing for genetic causes of a patient’s condition, or for preventative testing and treatment due to family history, HNL Genomics has convenient, accessible testing options that you and your patients need.

Frequently Ordered Cardiology Tests

We offer NGS and chromosome microarray (SNP array) for the most common cardiovascular conditions and more. Some of our most common tests include:

Whether your patients need testing for general prenatal care, inherited disease testing, or to investigate ultrasound abnormalities, HNL Genomics is committed to providing accurate, quality results, with best-in-industry turnaround times.

Our team is dedicated to serving your laboratory testing needs.

We offer Carrier Screening, Noninvasive prenatal screening (NIPS), and diagnostic prenatal testing for those with complicated medical or family histories. Our diagnostic offerings include a number of gene panels specifically focused on rare inherited diseases.

Frequently Ordered Prenatal Tests

HNL Genomics Inherited Genetics is an international provider specializing in molecular diagnostic testing services for hereditary genetic disorders.

The efficient systems and team of experts enable HNL Genomics to provide clear and actionable results, rapidly develop and deploy new tests, and offer superior customer service with the industry's best turn-around times. We use our proprietary analytic methods, mutation database, and technology to provide more than 3,300 unique tests covering over 1,000 genes.

Common Inherited Genetic disorders we test for:

Genomics Test Directory

Related Resources

Targeted and VUS Testing

Learn More about Targeted VUS Testing: Inherited Genetics.

Learn More

Variant Interpretation

Learn more about variant interpretation: Inherited Genetics.

Learn More

HNL Genomics Departments

Inherited Genetics

The Inherited Genetics division focuses on genetically- inherited disorders. A diagnosis of an inherited genetic disorder provides information on recurrence risk (in future generations) and allows for testing of family members. Click below to learn about the methods, technology and specialties of our Inherited Genetics team.

Learn More

Molecular Oncology:

Our Molecular Oncology division uses molecular testing to identify the genetic abnormalities that drive cancer and allows for targeted therapy and a better understanding of the patient's prognosis.

Learn More


HNL Lab Medicine’s Cytogenetics Lab performs the cytogenetics, fluorescence in situ hybridization (FISH) and chromosome microarray testing using the most advanced technologies. Chromosome, and FISH testing helps identify the diagnosis, prognosis and monitoring of the treatment for oncologic malignancies.

Learn More

Specimens from Outside North America 

Please send genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl), preferably in TE solution. HNL Genomics does not recommend shipping whole blood or cultured cells from any location other than the United States, Canada, or Mexico.

Frequently Ordered Genetic Tests

NGS Solid Tumor with TMB and MSI 
Noninvasive Prenatal Screening
Carrier Screening