Our Products
From preventive screening to comprehensive genome sequencing.
What You Get
Included with every Genavli product
Disease Predisposition
Variants of interest linked to hereditary conditions
Pharmacogenomics
How your genes affect medication response
Ancestry Composition
Your genetic heritage and population breakdown
Maternal Lineage (mtDNA)
Mitochondrial haplogroup and maternal ancestry
Carrier Screening
Recessive condition carrier status for family planning
Variant Explorer
Research-grade variant browser with annotations
Diagnostic-Grade Analysis
Additional features with our diagnostic tests
ACMG Classification
Clinical variant classification following ACMG/AMP guidelines
Clinical PDF Report
Comprehensive clinical report suitable for healthcare providers
Expert Manual Curation
Each variant reviewed and curated by trained genomics analysts
Certified Geneticist Review
Final review and sign-off by a board-certified clinical geneticist
Priority Support
Dedicated support channel with faster response times
Whole Genome Advantage
Exclusive to our most comprehensive test
Non-coding Region Coverage
Full genome coverage including intergenic, intronic, and regulatory regions
Structural Variant Detection
Identify large-scale genomic rearrangements, inversions, and translocations
Copy Number Variant Analysis
Detect deletions and duplications across the entire genome
Star Allele Genotyping
Complete pharmacogenomic profiling with star allele calls for accurate metabolizer phenotype prediction
Repeat Expansion Detection
Identify trinucleotide and other repeat expansions linked to neurological and neuromuscular conditions
Difficult-to-Call Genes
Accurate genotyping of complex genes like CYP2B6, CYP2D6, CYP21A2, GBA, HBA, LPA, RH, and SMN that require whole genome data
Compare Tests
| Feature | Screening GenAssure Exome Contact us for pricing | Diagnostic Genavli Exome Contact us for pricing | Most Comprehensive Genavli Genome Custom pricing |
|---|---|---|---|
| Genetic Markers | ~70 lakh | ~70 lakh | ~300 crore |
| Ancestry Analysis | |||
| Carrier Screening | |||
| Pharmacogenetics | |||
| Online Interactive Report | |||
| AI Interpretation | |||
| Lifetime Updates | |||
| Clinical Variant Classification (ACMG) | |||
| Clinical PDF Report | |||
| Expert Manual Curation | |||
| Certified Geneticist Review | |||
| Priority Support | |||
| Non-coding Region Coverage | |||
| Structural Variant Detection | |||
| Copy Number Variant Analysis | |||
| Star Allele Genotyping (PGx) | |||
| Repeat Expansion Detection | |||
| Difficult-to-Call Genes (CYP2D6, GBA, SMN, etc.) | |||
| Turnaround Time | 4–6 weeks | 4–6 weeks | 6–8 weeks |