Home Tests Clinical Whole Exome Sequencing with report (CNV)

Clinical Whole Exome Sequencing with report (CNV)

Umm Al Hamam Al Gharbi, Riyadh - 145KM

Advanced genetic test that analyzes all protein-coding regions of the genome (the exome), where most disease-causing mutations occur. This test not only identifies single-gene variants but also includes a Copy Number Variation (CNV) report, providing deeper insights into genetic abnormalities.

When is it used?
1- For patients with complex, undiagnosed conditions where standard tests fail to provide answers
2- In cases with suspected rare or inherited genetic disorders
3- When comprehensive genetic information is needed to guide diagnosis and treatment

Why choose BGI-Xome™ cWES with CNV report?
1-Comprehensive Analysis: Detects both single-gene mutations and CNVs across thousands of genes
2- Clinical Insight: Provides a more complete genetic profile to support accurate diagnosis
3- Actionable Results: Helps physicians create tailored medical management and treatment plans

Note: You should consult your treating physician before making any medical decision.
Results should always be interpreted in consultation with a physician or certified genetic counselor.
At Genalive, we provide professional genetic consultation to support patients and families in understanding their results.