Understand genetic reports with AI.
Complex genomic reports shouldn't require a medical degree to understand. Our AI turns difficult genetic reports into clear, actionable explanations for patients, clinicians, and laboratories — alongside clinical care, never in place of it.
Zenvis is an educational and workflow-support tool. It does not diagnose patients or replace a physician or genetic counselor.
BRCA1 c.68_69delAG — PATHOGENIC▍
Built for the future of precision medicine
[ FIG. 02 — THE GAP ]
Genetic reports are becoming common.
Understanding them isn't.
“I don't know what this mutation means.”
“I don't have enough consultation time.”
“We generate reports but can't educate every patient.”
“Genomic medicine is growing faster than interpretation.”
[ FIG. 03 — THE PIPELINE ]
AI that makes genomics understandable.
- STEP 01
Upload report
PDF, HL7, or lab API feed — encrypted in transit.
- STEP 02
AI analysis
Variant context is matched against curated clinical literature.
- STEP 03
Plain-language explanation
Findings rewritten at a 7th-grade reading level, in 11 languages.
- STEP 04
Clinical summary
A structured brief for the ordering clinician or counselor.
- STEP 05
Patient-friendly insights
Context, next steps, and questions worth asking a provider.
- STEP 06
Share securely
Access expires, is logged, and never leaves encrypted storage.
[ FIG. 04 — CAPABILITIES ]
One platform, every step of the report's life.
Plain-language explanations
Every finding rewritten in clear, everyday terms.
Doctor summaries
Concise clinical briefs built for a busy visit.
Patient education
Context on what a gene does and why it matters.
Variant explanations
Clear notes on pathogenic, benign, and uncertain calls.
Clinical workflow support
Fits into existing intake and reporting workflows.
Encrypted storage
Reports encrypted at rest and in transit, always.
Report comparison
See what changed between two reports over time.
Export summaries
Download patient and clinician versions as PDF.
API for laboratories
Programmatic interpretation at intake scale.
Healthcare-grade security
Built to HIPAA and GDPR-aligned standards.
[ FIG. 05 — OUTCOMES ]
Built for both sides of the exam room.
For Patients
- Understand reports without medical jargon
- Reduce anxiety around uncertain results
- Prepare for the doctor visit ahead of time
- Learn the medical terminology as it comes up
- Know exactly what questions to ask
For Healthcare Providers
- Save consultation time on repeat explanations
- Improve communication with every patient
- Increase patient satisfaction scores
- Reduce repetitive baseline explanations
- Improve report-to-conversation workflow
[ FIG. 11 — WHO IT'S FOR ]
Eight roles. One shared report.
Genetic Testing Labs
Scalable report explanation and patient engagement at intake volume.
[ FIG. 06 — IN PRACTICE ]
From report to conversation, in five steps.
Upload report
Add a PDF or connect your lab's existing feed.
AI processes genetics
Variants are matched to current clinical literature.
Receive simplified explanation
A plain-language version, ready in under a minute.
Receive clinician summary
A structured brief for the ordering provider.
Discuss with a professional
Walk into the conversation already informed.
[ FIG. 07 — TRUST ]
Healthcare-grade privacy, by default.
Genetic data is among the most sensitive information a person owns. Every layer of Zenvis is designed around that fact — not added to the roadmap later.
[ FIG. 08 — ROADMAP ]
Where this is heading.
AI report interpretation
Plain-language and clinical summaries at scale.
Clinical decision support
Structured guidance embedded in provider workflows.
Population genomics
Aggregate, de-identified insight across cohorts.
Precision medicine platform
One layer connecting labs, clinics, and patients.
[ FIG. 12 — EARLY VOICES ]
From our pilot programs.
Illustrative feedback from early pilot cohorts, shared with permission.
“The plain-language summary gave our patients something to hold onto before their appointment, instead of a report full of terms nobody explained.”
“We generate hundreds of reports a week. Anything that helps a patient arrive already oriented changes the whole conversation.”
“I finally understood what my own result meant, in language I could repeat to my family.”
[ FIG. 09 — EARLY ACCESS ]
Join the future of genomic intelligence.
Be among the first hospitals, laboratories, clinicians, and patients shaping the next generation of AI-powered genomics.
- → No cost during early access
- → Direct line to the product team
- → Priority onboarding at general launch
[ FIG. 10 — QUESTIONS ]
Frequently asked.
Most standard genetic and genomic test reports from major laboratories, including carrier screening, pharmacogenomics, hereditary cancer panels, and whole exome summaries. Coverage is expanding throughout early access.
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