Home Tests Clinical Whole Exome Sequencing with report (CNV)

Clinical Whole Exome Sequencing with report (CNV)

Umm Al Hamam Al Gharbi, Riyadh - 145KM

Whole Exome Sequencing (WES) is an advanced genetic test that analyzes the protein-coding regions of your genes, known as the exome. These regions contain many of the genetic variants known to cause inherited disorders.

The test also includes Copy Number Variation (CNV) analysis, which detects gains or losses of genetic material. Combining WES with CNV analysis provides a more comprehensive view of genetic changes that may be associated with a medical condition.

Why Is This Test Important & What Can It Detect?
Identifies genetic variants associated with complex and inherited disorders
Helps provide a more accurate diagnosis for unexplained or undiagnosed conditions
Provides in-depth genetic insights that may support medical management, treatment decisions, and follow-up
Combines the detection of sequence variants with Copy Number Variations (CNVs) for more comprehensive genetic analysis
Who Is This Test Recommended For?

WES may be recommended for:

Patients with complex or unexplained symptoms
Individuals whose previous tests have not identified a clear underlying cause
Individuals with a family history of rare or inherited genetic disorders
Physicians seeking comprehensive genetic insights to support diagnosis and guide patient management
Why Choose Genalive?
Specialized expertise in advanced genetic testing
High-quality, reliable results performed according to recognized laboratory standards
Strict privacy and confidentiality of your genetic data
A clear and convenient journey from booking to receiving your results
Qualified medical and technical professionals
Book Your Test Today