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Medical information Clinical review pending

Cytogenetics

FISH NTRK 1 Gene Rearrangement Assay Test

The FISH NTRK 1 Gene Rearrangement Assay Test detects rearrangements in the NTRK1 gene using FISH technology. This test helps guide personalised cancer treatment strategies.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Formalin-fixed paraffin-embedded tissue block or three 4-micron sections on Poly L Lysine coated slides.
Results
Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required. Ensure the Genomics Clinical Information Requisition Form (Form 20) is completed and submitted with the sample.
Test priceKSh 14,040

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the FISH NTRK 1 Gene Rearrangement Assay Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Patients with specific types of cancer
  • ✓Patients with metastatic disease
  • ✓Patients with unusual tumor characteristics
  • ✓Patients resistant to standard therapies
  • ✓Patients being considered for targeted therapies
02

In plain language

What this test helps you understand

Identifies NTRK1 gene rearrangements, which can inform targeted therapy options for certain cancers.
The FISH NTRK 1 Gene Rearrangement Assay Test is a diagnostic tool used in oncology to detect rearrangements in the NTRK1 gene. These genetic alterations can influence the behavior of certain cancers, making it crucial for determining the most effective treatment strategies. The test employs Fluorescence In Situ Hybridization (FISH) technology, which allows for the visualization of genetic changes within tissue samples. This test specifically measures the presence of NTRK1 gene rearrangements located at 1q21.3. Identifying these alterations can provide valuable insights into the tumor's characteristics and help tailor targeted therapies for patients. Discussing the results with your oncologist is essential to understand the implications for your treatment plan.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo specific patient preparation is required. Ensure the Genomics Clinical Information Requisition Form (Form 20) is completed and submitted with the sample.
SampleFormalin-fixed paraffin-embedded tissue block or three 4-micron sections on Poly L Lysine coated slides.
MethodologyFluorescence In Situ Hybridization (FISH).
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects specific NTRK1 rearrangements. It does not detect all possible genetic alterations. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test uses FISH technology to detect rearrangements in the NTRK1 gene, which can affect cancer behavior and treatment options.
Identifying NTRK1 rearrangements can help determine if a patient might benefit from specific targeted cancer therapies.
A formalin-fixed paraffin-embedded tissue block or unstained slides are required for this test.
Results indicate the presence or absence of NTRK1 gene rearrangements. Your doctor will interpret these results in the context of your overall health.
Confirm with the laboratory before booking.
Please call or WhatsApp us at +254711564616 to book the test.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

Explore partnerships
09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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