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DNA Labs India

VCL Gene Cardiomyopathy, dilated type 1W NGS Genetic Test

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VCL Gene Cardiomyopathy, dilated type 1W NGS Genetic Test

Short Name: VCL Gene Cardiomyopathy Dilated Type 1W NGS Test

Also known as: Dilated Cardiomyopathy Type 1W, VCL-related Cardiomyopathy

VCL Gene Cardiomyopathy, dilated type 1W 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.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose VCL Gene Cardiomyopathy Dilated Type 1W by detecting mutations in the VCL gene using NGS technology, aiding in early diagnosis and management of the condition.

Test Code
5226
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
Step 1

Sample Collection

Clinical history review and genetic counseling session to draw a pedigree chart of affected family members.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or alternative methods as specified.

Step 3

Report Delivery

Sample transported to lab for NGS analysis; results delivered in 3-4 weeks.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and pedigree analysis recommended to assess family history and test implications.
2
During the Test:Blood sample collection via venipuncture; minimal discomfort expected.
3
After the Test:Results available in 3-4 weeks; follow-up consultation advised for interpretation and management.

About This Test

Who Should Get This Test

To diagnose VCL Gene Cardiomyopathy Dilated Type 1W by detecting mutations in the VCL gene using NGS technology, aiding in early diagnosis and management of the condition.

How to Prepare

  • Provide detailed clinical history
  • Undergo genetic counseling for pedigree analysis
  • Use appropriate sample type as specified

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Early genetic testing for VCL mutations is crucial for guiding treatment strategies and enabling family screening in cardiomyopathy cases."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture

Sample Stability

Blood samples stable for 48 hours at room temperature
Extracted DNA stable for longer periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Improper labeling

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the VCL gene associated with dilated cardiomyopathy type 1W.
📊

Positive

Mutation detected in VCL gene; consult cardiologist for management and family screening.

📊

Negative

No mutation detected; clinical correlation recommended if symptoms persist.

📊

Variant of uncertain significance

Genetic variant found but significance unclear; further testing or consultation advised.

⚠️ When to Consult a Doctor:

If experiencing symptoms of heart failure, have a family history of cardiomyopathy, or after receiving test results for personalized care.

Limitations

  • May not detect all genetic variants
  • Results require clinical correlation

Risks & Considerations

  • Bruising at puncture site
  • Rare infection risk
  • Minimal discomfort

Interfering Factors

  • Poor sample quality
  • Contamination during collection

Frequently Asked Questions

What is VCL Gene Cardiomyopathy Dilated Type 1W?
It is a genetic condition caused by mutations in the VCL gene, leading to dilated cardiomyopathy where the heart chambers enlarge and weaken, potentially causing heart failure.
What are the common symptoms of this condition?
Symptoms include shortness of breath, fatigue, swelling in legs/ankles/feet, irregular heartbeat, chest pain, dizziness, and fainting.
How is the VCL Gene Cardiomyopathy test performed?
The test uses Next Generation Sequencing (NGS) technology to analyze the VCL gene for mutations from a blood or DNA sample.
What is the cost of the test at DNA Labs India?
The test costs INR 20,000, with free home sample collection available across India.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities across India.
How long does it take to get the test results?
Results are typically delivered within 3 to 4 weeks after sample collection.
What sample is required for the test?
The test requires blood, extracted DNA, or one drop of blood on an FTA card.
Do I need genetic counseling before the test?
Yes, genetic counseling is recommended to draw a pedigree chart of family members and understand the test implications.
What does a positive test result mean?
A positive result indicates a mutation in the VCL gene, suggesting a diagnosis of VCL Gene Cardiomyopathy Dilated Type 1W; consult a cardiologist for management.
Can this test be used for family screening?
Yes, if a mutation is identified, family members can be tested for early detection and preventive care.
Is the test covered by insurance schemes like PMJAY or CGHS?
Coverage varies; it is not typically covered, but check with specific schemes for eligibility.
Why choose DNA Labs India for this genetic test?
DNA Labs India offers accurate NGS testing, affordable pricing, free home collection, and transparency by sharing raw data files with clinical reports.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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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.

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