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DNA Labs India

FISH - RARA (17q21) Variant Translocation Test

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FISH - RARA (17q21) Variant Translocation Test

Short Name: RARA Variant Translocation FISH

Also known as: RARA break-apart probe test, Variant RARA translocation FISH, FISH for RARA gene rearrangement

FISH - RARA (17q21) Variant Translocation Test test available at DNA Labs India for ₹6,000. Uses Fluorescence in situ hybridization (FISH) on Whole blood or Bone marrow samples. Results in Reports available within 4 days from sample receipt.. Free home collection in 300+ cities across India.

FISH Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect variant RARA gene translocations that are not identified by standard FISH tests, aiding in the diagnosis and treatment planning for acute promyelocytic leukemia (APL).

Test Code
598
Price
₹6,000
Sample Type
Whole blood or Bone marrow
Result Time
Reports available within 4 days from sample receipt.
Fasting Required
No
Method
Fluorescence in situ hybridization (FISH)
Step 1

Sample Collection

Ensure the Chromosome & FISH analysis Requisition Form (Form 17) is duly filled. No specific preparation is required.

Method: Venipuncture for blood, Bone marrow aspiration

Step 2

Laboratory Analysis

Sample is collected via venipuncture for blood or bone marrow aspiration, placed in sodium heparin tubes.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bleeding. Keep the sample at room temperature.

Timeline: Reports available within 4 days from sample receipt.

Patient Instructions

1
Before the Test:Complete the mandatory requisition form. No fasting is required.
2
During the Test:Sample collection takes a few minutes. The test is performed in a laboratory using FISH technology.
3
After the Test:Resume normal activities. Monitor the collection site for any discomfort.

About This Test

Who Should Get This Test

The purpose of this test is to detect variant RARA gene translocations that are not identified by standard FISH tests, aiding in the diagnosis and treatment planning for acute promyelocytic leukemia (APL).

How to Prepare

  • Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory
  • Collect 5 mL whole blood or 4 mL bone marrow in 2 Green Top (Sodium Heparin) tubes
  • Ship sample at 18-22°C; do not freeze

Doctor's Notes

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

"This test is essential for diagnosing variant RARA translocations in APL, guiding targeted therapy and improving patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole blood or Bone marrow
Sample Volume5 mL whole blood (3 mL min.) or 4 mL bone marrow (2 mL min.)
Container2 Green Top (Sodium Heparin) tubes
Collection MethodVenipuncture for blood, Bone marrow aspiration

Sample Stability

Room Temperature: 48 hours
Refrigerator: Not applicable
Frozen: Not applicable
Sample Rejection Criteria:
  • Insufficient sample volume
  • Improper container or anticoagulant
  • Sample not shipped at correct temperature
  • Missing or incomplete requisition form

Understanding Your Results

Results indicate whether variant RARA translocations are detected. A positive result confirms the presence of a genetic abnormality linked to APL.
📊

Negative

No variant RARA translocation detected. Correlate with clinical findings.

📊

Positive

Variant RARA translocation detected, suggesting acute promyelocytic leukemia (APL). Requires further clinical evaluation.

⚠️ When to Consult a Doctor:

Consult a hematologist or oncologist if the test is positive or if symptoms of leukemia persist. Discuss results for appropriate treatment planning.

Limitations

  • May not detect all rare variant translocations
  • Requires skilled interpretation by a cytogeneticist
  • Not a standalone diagnostic; clinical correlation is needed

Risks & Considerations

  • Minor bruising or pain at the collection site
  • Rare risk of infection with bone marrow aspiration

Interfering Factors

  • Poor sample quality or insufficient volume
  • Improper sample collection or storage
  • Contamination during processing

Frequently Asked Questions

What is the FISH - RARA (17q21) Variant Translocation Test?
It is a genetic test using FISH technology to detect variant translocations in the RARA gene, associated with acute promyelocytic leukemia (APL).
Why is this test recommended?
It is recommended when standard tests for t(15;17) are negative but APL is suspected, to identify variant translocations for accurate diagnosis.
What sample is required for this test?
5 mL of whole blood or 4 mL of bone marrow collected in sodium heparin tubes.
Is fasting required before the test?
No, fasting is not required for this test.
How long does it take to get results?
Results are typically available within 4 days from sample receipt.
What does a positive result mean?
A positive result indicates the presence of a variant RARA translocation, suggesting acute promyelocytic leukemia (APL). Further clinical evaluation is needed.
What does a negative result mean?
A negative result means no variant RARA translocation was detected. Correlate with clinical symptoms and other tests.
Is the test covered by insurance?
Coverage depends on your insurance policy. Contact your provider for details.
Are there any risks associated with the test?
Risks are minimal, such as bruising at the collection site or rare infection with bone marrow aspiration.
How should I prepare for the test?
Complete the mandatory requisition form (Form 17) and ensure proper sample collection. No special preparation is needed.
What cities offer home sample collection?
Home collection is available in major cities across India, including Mumbai, Delhi, Bangalore, and many more. Check our website for the full list.
Can this test be used for monitoring treatment?
Yes, it can help monitor treatment response in patients with APL by detecting changes in translocation status.
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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Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

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