Natera
Featured partnerUncover what genetic coding is driving my cancer, especially those variants of interest that can be targeted for treatment
Get started with Natera
How to get started
Upload your records
Pathology, genomics, imaging — whatever you have. We extract the clinical details automatically so nothing gets retyped. Upload records →
Share with Natera
We package your records into a secure, HIPAA-compliant bundle and pre-fill the intake. You review and sign — that's it. Share records →
Natera reaches out
Their team confirms next steps directly with you — testing, scheduling, consultation, or enrollment.
About this service
Uncover what genetic coding is driving my cancer, especially those variants of interest that can be targeted for treatment
DNA sequencing: mapping and analysis of tumor tissue for DNA variants, whole exome raw data best if a personalized vaccine being considered
Coverage, insurance & cost
The fastest way to know what you'll pay: check your coverage with your plan. Below is what we know about how Natera handles billing.
Accepted
Available
Required
In-network carriers
Who this is for
Cancer types served
Generally requires prior treatment history — eligibility confirmed during intake.
Common questions in this category
Based on what other patients have asked.
When is a pet/ct scan advised for a new breast cancer diagnosis
Breast CancerDoes the specific variant of the CHEk2 mutation make a difference? I have the Ashkenazi Founder variant.
Is the CHEK2 mutation related to prostate cancer
What should I know as a newly diagnosed CRC patient
Colorectal CancerWhat should I ask my oncologist after a new diagnosis
What are all the KRAS mutations, how are they categorized
Ovarian CancerAlso consider
Other providers in similar categories.
BostonGene
5 offeringsProvide an integrated profile of the disease at maximum depth to identify novel personalized treatment options and guide strategy and decisions
Tempus
5 offeringsTempus xT is a comprehensive genomic profiling test combining DNA and RNA sequencing to identify actionable mutations.
Foundation Medicine
4 offeringsFoundationOne CDx is an FDA-approved comprehensive genomic profiling test that analyzes 324 genes to identify clinically relevant genomic alterations.
Protean Biodiagnostics
3 offeringsFinds clinical trials you actually qualify for — matched to your tumor's biomarkers and treatment history, not a generic keyword search.
Get personalized guidance for your case
This page is general information. Upload your records for analysis specific to YOUR diagnosis.