CeGaT US Insurance Options

Benefit from our network with various commercial insurers

At CeGaT, we combine our expertise in genetics with the latest technology to make diagnosing patients easy and accessible. Providing a range of affordable services that supports our patients, physicians, and healthcare partners every step of the way, we accelerate diagnoses and treatment options.

To offer you affordable options, we partnered with various commercial insurers, like BlueCross BlueShield®, and many more. Find here more of our options.

Your Local Contact

Eric R. Miller

Head of Business Development and Sales – North America

CeGaT Corporation
2430 N-Halsted #110 | Chicago, IL 60614
Mobile: 312.287.7545
Phone: 312.783.5225
Fax: 773.828.3704
Email: eric.miller@cegat.com

Anil Bhardwaj

Head of Sales and Business Development – North America

CeGaT Corporation
2430 N-Halsted #110 | Chicago, IL 60614
Mobile: +44 7500 081932
Phone: 312.783.5225
Fax: 773.828.3704
Email: anil.bhardwaj@cegat.com

The CeGaT Advantage

Our comprehensive suite of services is designed to be both accessible and affordable, ensuring that patients, physicians, and healthcare partners receive unwavering support throughout the diagnostic journey. We offer a broad range of options to support you in your diagnostic journey.

Medicaid
All patients deserve the right to access genetic testing, regardless of ability to pay. Contact your local CeGaT representative for further details.

Medicare and TriCare (East/West)
Flat rate co-payment for Medicare or TriCare patients. (excluding Medicare Advantage Plans)

Low Maximum Out-of-Pocket Costs
Patients with eligible commercial & Medicare Advantage insurance plans pay less. Contact your local CeGaT representative for further details.

Variety of Financial Assistance Programs Available
For those with ineligible commercial insurance or who have suffered financial hardship.

If you need further support or have questions relating to financial assistance, contact our CeGaT Billing Team at 888.454.9136 or CeGaTbilling@plenummd.com

Diagnostic Service Overview

We offer a broad range of genetic tests in the area of rare diseases and tumor diseases, such as or our self-developed ExomeXtra®.

Diagnostic Panels for Rare Diseases

Using the latest molecular genetic methods, we determine the cause of the disease.

  • Blood Disorders
  • Cardiac Diseases
  • Ciliopathies
  • Connective Tissue Diseases
  • Epilepsy & Brain Development
  • Disorders
  • Eye Diseases
  • Fertility
  • Hearing Loss
  • Immune Disorders
  • Kidney Diseases
  • Liver Diseases
  • Metabolic Diseases incl. Mitochondriopathies
  • Neurodegenerative Diseases
  • Neuromuscular Diseases
  • Skeletal Disorders
  • Skin Diseases
Tumor Diseases

Genetic tumor diagnostics provides the information basis for treatment decisions.

  • Hereditary Tumor Syndromes
    Analysis of all known genes associated with hereditary tumor syndromes
  • CancerEssential®
    Evaluate the suitability of planned therapies for the most common tumor entities
  • CancerPrecision®
    Comprehensive diagnostics for targeted cancer treatment
  • CancerFusionRx®
    RNA-based identification of fusion transcripts
  • CancerNeo®
    Identify neoantigens for personalized cancer vaccine design
  • CancerDetect®
    Highly sensitive detection of actionable variants from liquid biopsy with low tumor content
  • CancerAdvice
    Precise recommendations on targeted therapies
CeGaT ExomeXtra®

Better than exome – smarter than genome

  • All protein-coding regions of the genome
  • Clinically relevant RNA genes
  • > 38,000 intergenic and intronic positions associated with genetic disease according to ClinVar, HGMD, and internal databases
  • High and uniform coverage of the entire mitochondrial genome to reliably detect different degrees of heteroplasmy
  • Pharmacogenetically relevant variants in selected genes
  • Backbone for genome-wide detection of copy number variants (CNVs)

Diagnostic Service Overview

Diagnostic Panel for Rare Diseases

Using the latest molecular genetic methods, we determine the cause of the disease.

  • Blood Disorders
  • Cardiac Diseases
  • Ciliopathies
  • Connective Tissue Diseases
  • Epilepsy & Brain Development
  • Disorders
  • Eye Diseases
  • Fertility
  • Hearing Loss
  • Immune Disorders
  • Kidney Diseases
  • Liver Diseases
  • Metabolic Diseases incl. Mitochondriopathies
  • Neurodegenerative Diseases
  • Neuromuscular Diseases
  • Skeletal Disorders
  • Skin Diseases

Tumor Diseases

Genetic tumor diagnostics provides the information basis for treatment decisions.

  • Hereditary Tumor Syndromes
    Analysis of all known genes associated with hereditary tumor syndromes
  • CancerEssential®
    Evaluate the suitability of planned therapies for the most common tumor entities
  • CancerPrecision®
    Comprehensive diagnostics for targeted cancer treatment
  • CancerFusionRx®
    RNA-based Fusion Detection
  • CancerNeo®
    Identify neoantigens for personalized cancer vaccine design
  • CancerDetect®
    Highly sensitive detection of actionable variants from liquid biopsy with low tumor content
  • CancerAdvice
    Precise recommendations on targeted therapies

CeGaT ExomeXtra®

Better than exome – smarter than genome

  • All protein-coding regions of the genome
  • Clinically relevant RNA genes
  • > 38,000 intergenic and intronic positions associated with genetic disease according to ClinVar, HGMD, and internal databases
  • High and uniform coverage of the entire mitochondrial genome to reliably detect different degrees of heteroplasmy
  • Pharmacogenetically relevant variants in selected genes
  • Backbone for genome-wide detection of copy number variants (CNVs)

Diagnostic Service Overview

Diagnostic Panel for Rare Diseases

Using the latest molecular genetic methods, we determine the cause of the disease.

  • Blood Disorders
  • Cardiac Diseases
  • Ciliopathies
  • Connective Tissue Diseases
  • Epilepsy & Brain Development
  • Disorders
  • Eye Diseases
  • Fertility
  • Hearing Loss
  • Immune Disorders
  • Kidney Diseases
  • Liver Diseases
  • Metabolic Diseases incl. Mitochondriopathies
  • Neurodegenerative Diseases
  • Neuromuscular Diseases
  • Skeletal Disorders
  • Skin Diseases

Tumor Diseases

Genetic tumor diagnostics provides the information basis for treatment decisions.

  • Hereditary Tumor Syndromes
    Analysis of all known genes associated with hereditary tumor syndromes
  • CancerEssential®
    Evaluate the suitability of planned therapies for the most common tumor entities
  • CancerPrecision®
    Comprehensive diagnostics for targeted cancer treatment
  • CancerFusionRx®
    RNA-based Fusion Detection
  • CancerNeo®
    Identify neoantigens for personalized cancer vaccine design
  • CancerDetect®
    Highly sensitive detection of actionable variants from liquid biopsy with low tumor content
  • CancerAdvice
    Precise recommendations on targeted therapies

CeGaT ExomeXtra®

Better than exome – smarter than genome

  • All protein-coding regions of the genome
  • Clinically relevant RNA genes
  • > 38,000 intergenic and intronic positions associated with genetic disease according to ClinVar, HGMD, and internal databases
  • High and uniform coverage of the entire mitochondrial genome to reliably detect different degrees of heteroplasmy
  • Pharmacogenetically relevant variants in selected genes
  • Backbone for genome-wide detection of copy number variants (CNVs)

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