CRB2 Gene Ventriculomegaly with cystic kidney disease NGS Genetic Test
CRB2 Gene Ventriculomegaly with cystic kidney disease NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the CRB2 Gene NGS Genetic Test is to detect mutations in the CRB2 gene to confirm a diagnosis of ventriculomegaly with cystic kidney disease, enabling appropriate medical management and genetic counseling.
- Test Code
- 4599
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
A certified phlebotomist visits your home or you visit our nearest center. The process takes under 5 minutes.
Laboratory Analysis
Your sample is analyzed using NGS Technology in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the CRB2 Gene NGS Genetic Test is to detect mutations in the CRB2 gene to confirm a diagnosis of ventriculomegaly with cystic kidney disease, enabling appropriate medical management and genetic counseling.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of CRB2-related ventriculomegaly with cystic kidney disease. Genetic counseling and symptom management recommended.
Negative for pathogenic variant
No CRB2 gene mutations detected. Consider other genetic or non-genetic causes based on clinical symptoms.
Variant of uncertain significance (VUS)
Genetic variant identified but clinical significance unknown. Further testing and family studies may be needed.
Consult a doctor if symptoms such as enlarged brain ventricles, cystic kidneys, developmental delays, or seizures are present, or if there is a family history of similar conditions.
Risks & Considerations
- ●Minor bruising or discomfort at blood draw site
- ●Rare risk of infection
- ●Emotional impact of genetic results
Frequently Asked Questions
What is the CRB2 Gene NGS Genetic Test?
Who should consider this test?
What is the cost of the test in India?
How is the sample collected?
Is fasting required before the test?
How long does it take to get results?
What does a positive result mean?
Is the test accurate?
Are there any risks associated with the test?
Can the test be done at home?
What treatment options are available after diagnosis?
Is genetic counseling recommended?
Related Tests
Angelman Syndrome Test
₹10,000Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test
₹14,000Episodic Ataxia Type 1 Hotspot Test
₹11,500Episodic Ataxia Comprehensive Profile Hotspot Test
₹16,000Megalencephalic Leukoencephalopathy with Subcortical Cysts Van Der Knaap and Nalband MLC Gene Hotspot Mutation Test
₹7,500Analyzer 18 SMA 18 Test Panel
₹1,755Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
Book Your Test
Enter your details and we'll connect you within 15 minutes.