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DES Gene Cardiomyopathy, dilated type 1I NGS Genetic Test

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DES Gene Cardiomyopathy, dilated type 1I NGS Genetic Test

Short Name: DES Gene DCM Type 1I NGS Test

Also known as: Dilated Cardiomyopathy with Desmin-related Myopathy

DES Gene Cardiomyopathy, dilated type 1I 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 Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect mutations in the DES gene associated with dilated cardiomyopathy type 1I, aiding in accurate diagnosis, risk assessment, family planning, and personalized treatment strategies for affected individuals.

Test Code
5214
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

No specific preparation required. Provide clinical history and family pedigree information during genetic counseling.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture or a drop on FTA card by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless otherwise advised.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling to understand the test implications, provide family history, and sign informed consent.
2
During the Test:A small blood sample is drawn; the procedure is quick and minimally invasive, typically taking a few minutes.
3
After the Test:Results are available in 3-4 weeks. Follow up with your doctor to discuss findings and next steps.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the DES gene associated with dilated cardiomyopathy type 1I, aiding in accurate diagnosis, risk assessment, family planning, and personalized treatment strategies for affected individuals.

How to Prepare

  • Ensure proper identification and labeling of samples
  • Use sterile equipment to avoid contamination
  • Follow standard phlebotomy procedures
  • Store samples appropriately before transport

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for DES gene mutations is crucial for early diagnosis, family screening, and management of dilated cardiomyopathy, especially in individuals with a family history of heart failure."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
ContainerEDTA tube for blood samples
Collection MethodVenipuncture

Sample Stability

Blood samples stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of mutations in the DES gene. Positive results suggest a genetic predisposition to dilated cardiomyopathy type 1I, while negative results may not completely exclude the condition due to other genetic or environmental factors.
📊

Positive for DES gene mutation

Confirms genetic basis for dilated cardiomyopathy; recommend cardiac evaluation, family screening, and genetic counseling.

📊

Negative for DES gene mutation

No pathogenic mutation detected in the DES gene; consider other genetic or non-genetic causes if symptoms persist.

📊

Variant of uncertain significance (VUS)

A genetic variant was found but its clinical significance is unknown; further testing and monitoring may be needed.

⚠️ When to Consult a Doctor:

Consult a cardiologist or genetic specialist if you experience symptoms of heart failure, have a family history of cardiomyopathy, or receive a positive genetic test result for guidance on management and family screening.

Limitations

  • May not detect all genetic variants or mutations in the DES gene
  • Results require clinical correlation and genetic counseling
  • Does not rule out other causes of cardiomyopathy
  • Limited to known mutations in the DES gene based on current databases

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or infection
  • Psychological impact of genetic results may require counseling

Interfering Factors

  • Hemolyzed or degraded DNA samples may affect test accuracy
  • Recent blood transfusions could interfere with genetic analysis
  • Contamination during sample collection or processing

Compare With Similar Tests

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ComparisonDES Gene Cardiomyopathy, dilated type 1I NGS Genetic Test

Frequently Asked Questions

What is the DES Gene Cardiomyopathy NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to detect mutations in the DES gene associated with dilated cardiomyopathy type 1I, a rare heart condition.
Who should consider this test?
Individuals with symptoms of heart failure, a family history of dilated cardiomyopathy, or those diagnosed with unexplained cardiomyopathy should consider this test.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to identify mutations in the DES gene.
What is the cost of the test in India?
The test costs INR 20000 at DNA Labs India, with free home sample collection available across many cities.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
Results indicate the presence or absence of DES gene mutations. Positive results suggest a genetic predisposition to cardiomyopathy, while negative results may require further evaluation.
Is the test accurate?
The test uses advanced NGS technology for high accuracy, but results should be interpreted by a healthcare professional in clinical context.
Can the test be done at home?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
What are the risks of the test?
Risks are minimal, primarily related to blood draw, such as bruising. Genetic results may have psychological impacts, so counseling is recommended.
Is the test covered by insurance?
Coverage varies by insurance provider; it is not typically covered under government schemes like PMJAY or CGHS. Check with your insurer.
How do I prepare for the test?
No special preparation is needed. Provide your clinical history and family pedigree during genetic counseling before the test.
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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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.

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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.

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