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DNA Labs India

Myeloid tumor panel NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

Myeloid tumor panel NGS Genetic Test

Short Name: Myeloid Tumor Panel NGS

Also known as: Myeloid Neoplasm NGS Panel, Myeloid Cancer Genetic Panel, NGS Panel for Myeloid Disorders

Myeloid tumor panel NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) 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.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Myeloid Tumor Panel NGS Genetic Test is to detect mutations in genes commonly associated with myeloid tumors, enabling precise diagnosis, risk stratification, and targeted therapy selection. It helps in identifying actionable mutations that may respond to specific treatments, improving patient outcomes and reducing unnecessary therapies.

Test Code
2825
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
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation is required. Ensure to provide clinical history and undergo genetic counseling as recommended.

Method: Venipuncture or fingerstick

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm or a fingerstick for FTA card. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately. Results will be available in 3-4 weeks.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling to understand the test implications. Provide detailed clinical and family history.
2
During the Test:Sample collection takes about 10-15 minutes. The sample is processed in the lab using NGS technology.
3
After the Test:Wait for 3-4 weeks for results. Discuss findings with your doctor for next steps.

About This Test

Who Should Get This Test

The purpose of the Myeloid Tumor Panel NGS Genetic Test is to detect mutations in genes commonly associated with myeloid tumors, enabling precise diagnosis, risk stratification, and targeted therapy selection. It helps in identifying actionable mutations that may respond to specific treatments, improving patient outcomes and reducing unnecessary therapies.

How to Prepare

  • Fast for 8-12 hours if specified, though not typically required
  • Avoid strenuous exercise before sample collection
  • Inform the phlebotomist of any medications or recent transfusions
  • Ensure proper labeling of the sample with patient details

Doctor's Notes

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

"This test is crucial for personalized treatment planning in myeloid tumors, helping to identify targetable mutations and improve patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood or equivalent
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or fingerstick

Sample Stability

Blood sample: Stable for 24 hours at room temperature
Extracted DNA: Stable for several days if stored properly
FTA card: Stable at room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Incorrect sample type or container
  • Missing patient identification or consent

Understanding Your Results

Results from the Myeloid Tumor Panel NGS Genetic Test indicate the presence or absence of mutations in the tested genes. A positive result means a mutation was detected, which may guide treatment decisions, while a negative result suggests no mutations in the panel genes.
Mutation detected: Consult with an oncologist for targeted therapy options
No mutation detected: Consider other diagnostic tests or clinical evaluation
Variant of uncertain significance (VUS): May require further testing or monitoring
Results should be correlated with clinical symptoms and other lab findings
⚠️ When to Consult a Doctor:

Consult your doctor immediately if you experience symptoms like persistent fatigue, unexplained weight loss, or abnormal bleeding. After receiving test results, discuss them with your oncologist or geneticist for personalized management.

Limitations

  • May not detect all rare or novel mutations
  • Cannot replace comprehensive clinical evaluation
  • Results require interpretation by a qualified geneticist or oncologist
  • Limited to genes included in the panel; other genetic factors may not be assessed

Risks & Considerations

  • Minimal risk from blood draw, such as slight pain or bruising
  • Psychological impact of genetic results; counseling is provided
  • No significant physical risks associated with the test itself

Interfering Factors

  • Sample contamination or degradation
  • Insufficient sample volume
  • Recent blood transfusions affecting DNA quality
  • Use of certain medications that may alter genetic expression

Compare With Similar Tests

TestMyeloid tumor panel NGS Genetic TestMyelodysplastic Syndrome (MDS) PanelAcute Lymphoblastic Leukemia (ALL) PanelComprehensive Cancer PanelSingle Gene Testing (e.g., FLT3 alone)
ComparisonMyeloid tumor panel NGS Genetic Test

Frequently Asked Questions

What is the Myeloid Tumor Panel NGS Genetic Test?
It is a diagnostic test using next-generation sequencing to detect mutations in genes associated with myeloid tumors, such as FLT3 and NPM1.
Why is this test important?
It provides genetic insights for accurate diagnosis, prognosis, and personalized treatment of myeloid tumors like AML.
What symptoms indicate the need for this test?
Symptoms include fatigue, fever, weight loss, bone pain, easy bruising, or enlarged lymph nodes.
How is the test performed?
A blood or bone marrow sample is collected and analyzed using NGS technology in a laboratory.
What is the cost of the test in India?
The cost is INR 20000, with free home sample collection available across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
Is fasting required before the test?
No, fasting is not required for this test.
What genes are tested in this panel?
Genes include FLT3, NPM1, IDH1, IDH2, ASXL1, TP53, RUNX1, TET2, and others listed in the parameters.
Can this test detect all myeloid tumor mutations?
It covers a comprehensive panel but may not detect all rare mutations; consult your doctor for limitations.
Is genetic counseling included?
Yes, DNA Labs India includes genetic counseling to help interpret results.
What should I do after receiving the results?
Discuss the results with your oncologist or geneticist to plan treatment or further testing.
Is the test available in my city?
Yes, free home collection is available in numerous cities across India, including Mumbai, Delhi, Bangalore, and more.
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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For Hospitals & Clinics

Reference 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.

LIMS Integration

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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