Hereditary cardiovascular
Guide diagnosis and management of cardiovascular disorders through your patient’s genetic insights.
sequence once, query often®
TURNAROUND
Existing Patient (SOQO)Ⓡ< 5 days
TURNAROUND
New Patient6-21 days
SAMPLE
Saliva, Blood, Buccal
One comprehensive test provides clinical answers today and enables future queries as science evolves.
If your patient has been sequenced before, Helix will automatically flag them as an existing patient in your EHR ordering workflow. No new sample required.
Clinical Utility
Identifies individuals with hereditary cardiac conditions who may benefit from:
- Increased cardiac screening
- Risk-reducing medical treatments
- Targeted therapies
- Clarification of risk for family members
TECH SPECS
Methodology
Exome+® NGS (exome capture + deep intronic coverage in key regions + relevant promoters and inversions).
Accuracy
> 99.9% analytical sensitivity for SNVs and small indels.
CNV resolution
Single exon-level resolution for deletions and duplications.
Wayfinder™ interpretation
Automated pathogenicity scoring powered by 3M+ longitudinal records and AI synthesis for superior intelligence.
Test Catalog
Select a test below to view a detailed test description, technical specifications and complete gene list.
Comprehensive Cardiomyopathy Panel
An 86-gene panel for assessing cardiomyopathy and associated syndromic conditions, powered by the He...
86
genesComprehensive Cardiomyopathy and Arrhythmias Panel
A comprehensive 103-gene panel for assessing cardiomyopathy, arrhythmia, and associated syndromic co...
103
genesComprehensive Arrhythmias Panel
A 39-gene panel for evaluating hereditary arrhythmia and associated syndromic conditions, powered by...
39
genesHypertrophic Cardiomyopathy Panel
A 47-gene panel for evaluating hereditary hypertrophic cardiomyopathy, powered by the Helix Exome+® ...
47
genes