Skip to main content
Medical information Clinical review pending

Cytogenetics

FISH Follicular Lymphoma IGHBCL2 t14;18 Test

The FISH Follicular Lymphoma IGHBCL2 t14;18 Test helps identify a specific genetic change associated with follicular lymphoma, aiding in diagnosis and treatment planning.

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.

Ask a question
Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
4 mL (3 mL min.) whole blood OR 4 mL (2 mL min.) Bone marrow from 2 Green Top (Sodium Heparin) tubes OR Lymph node biopsy (5x5 mm) in normal saline OR Formalin fixed paraffin embedded tissue block.
Results
Reports are typically available within 4 working days after sample receipt.
Preparation
Confirm with the laboratory before booking. Specific preparation instructions may vary depending on the sample type.
Test priceKSh 18,000

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 Follicular Lymphoma IGHBCL2 t14;18 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.

+254

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.

  • ✓Diagnosis of suspected follicular lymphoma
  • ✓Characterization of non-Hodgkin lymphoma
  • ✓Monitoring disease progression
  • ✓Guiding treatment strategies
  • ✓Evaluating patients with lymph node enlargement
  • ✓Assessing patients with lymphoma symptoms
02

In plain language

What this test helps you understand

This test is used to detect the IGH/BCL2 gene rearrangement, a specific genetic marker associated with follicular lymphoma. It aids in confirming the diagnosis and guiding treatment decisions.
The FISH Follicular Lymphoma IGHBCL2 t14;18 Test is a specialized diagnostic tool used to detect genetic abnormalities linked to follicular lymphoma, a common type of non-Hodgkin lymphoma. This test is vital for oncologists in determining the best treatment strategies for patients diagnosed with this disease.

This test specifically measures the presence of the IGH/BCL2 gene rearrangement, which is indicative of follicular lymphoma. By identifying these genetic changes, healthcare providers can better understand the nature of the disease and its progression.

Patients experiencing symptoms such as swollen lymph nodes, unexplained weight loss, fever, or night sweats should consider this test. Additionally, individuals with a family history of lymphomas or those at higher risk due to other medical conditions may also benefit from testing.

Benefits of taking this test include accurate diagnosis of follicular lymphoma, informing treatment decisions tailored to the patient's specific condition, and helping in monitoring disease progression and response to therapy.

Results from the FISH Follicular Lymphoma IGHBCL2 t14;18 Test will indicate whether the IGH/BCL2 gene rearrangement is present. A positive result confirms the presence of follicular lymphoma, while a negative result may suggest a different diagnosis. It is essential to discuss your results with your oncologist for appropriate interpretation and management.
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 →
PreparationConfirm with the laboratory before booking. Specific preparation instructions may vary depending on the sample type.
Sample4 mL (3 mL min.) whole blood OR 4 mL (2 mL min.) Bone marrow from 2 Green Top (Sodium Heparin) tubes OR Lymph node biopsy (5x5 mm) in normal saline OR Formalin fixed paraffin embedded tissue block.
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 a specific genetic rearrangement. A negative result does not rule out lymphoma, and further testing may be required. Interpretation requires clinical correlation.
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

Follicular lymphoma is a common type of non-Hodgkin lymphoma, a cancer that starts in the lymphatic system.
This test helps confirm the diagnosis of follicular lymphoma by detecting a specific genetic change (IGH/BCL2 rearrangement), which is crucial for planning appropriate treatment.
Samples can include whole blood, bone marrow, lymph node tissue, or formalin-fixed paraffin-embedded tissue blocks. Please confirm requirements with the lab.
Results are typically available within 4 working days after the laboratory receives the sample.
Your doctor or oncologist will interpret the results in the context of your overall health and clinical picture.
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.

Keep exploring

Related tests

View all tests →
Chat on WhatsApp