VarSeq is the leading platform for interpreting genomic variants in clinical practice. Unlock actionable insights for rare disease diagnosis, cancer genomics, and carrier screening.
From rare disease diagnosis to cancer genomics, VarSeq provides the tools clinicians and researchers need to interpret genetic variants with confidence.
Accelerate diagnosis of rare genetic disorders with intelligent variant prioritization and comprehensive phenotype matching.
Identify clinically actionable variants in cancer samples with precision oncology interpretations and treatment recommendations.
Assess familial risk with advanced penetrance and expression analysis for hereditary cancer and disease predisposition syndromes.
Comprehensive carrier screening for reproductive health with expanded genetic panels and actionable recommendations.
VarSeq combines advanced variant annotation, evidence-based interpretation, and clinical decision support to deliver rapid, accurate insights.
Population frequencies, functional predictions, and clinical evidence from thousands of data sources.
Automated variant classification following the latest ACMG/AMP guidelines with transparent reasoning.
Generate professional, publication-ready reports with customizable templates for your laboratory.
Secure sharing and real-time collaboration for multidisciplinary team-based variant interpretation.
Variants Analyzed
Clinical Labs
Uptime SLA
Support
Join leading clinical laboratories using VarSeq for variant interpretation and clinical decision support.