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Medical information Clinical review pending

Infection Testing

Xpert Xpress SARS-CoV-2 Qualitative Test

The Xpert Xpress SARS-CoV-2 Qualitative Test is a rapid molecular test using Real-Time PCR to detect the SARS-CoV-2 virus, which causes COVID-19. It provides quick results for individuals with symptoms or exposure.

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
Nasopharyngeal swab, Nasal wash swab, or Aspirate specimen collected in a special Viral transport medium (VTM). Confirm with the laboratory before booking.
Results
Same-day report if the sample is received by 11 am. Confirm with the laboratory before booking.
Preparation
No specific preparation is required for this test. Follow collection instructions provided by the healthcare provider or laboratory.
Test priceKSh 5,616

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 Xpert Xpress SARS-CoV-2 Qualitative 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.

  • ✓Individuals experiencing symptoms of COVID-19 (e.g., fever, cough, loss of taste/smell).
  • ✓Individuals with known close contact to confirmed COVID-19 cases.
  • ✓Testing required for travel or regulatory purposes.
  • ✓Screening in specific settings as recommended by public health guidelines.
02

In plain language

What this test helps you understand

This test is used to detect the presence of the SARS-CoV-2 virus in individuals suspected of having COVID-19, aiding in diagnosis and guiding management decisions.
The Xpert Xpress SARS-CoV-2 Qualitative Test is a diagnostic tool that uses Real-Time PCR technology to detect the presence of SARS-CoV-2, the virus responsible for COVID-19. This test is designed for individuals who are experiencing symptoms suggestive of COVID-19 or have been in close contact with confirmed cases. It allows for swift diagnosis and appropriate management.

This qualitative test specifically measures the presence of the SARS-CoV-2 virus in respiratory specimens. It is designed to provide accurate results in a short turnaround time, making it an essential tool in the fight against COVID-19.

Results from the Xpert Xpress SARS-CoV-2 Qualitative Test are reported as either positive or negative. A positive result indicates the presence of the virus, while a negative result suggests that the virus was not detected at the time of testing. It is essential to consult with a healthcare professional for further guidance based on your results.
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 preparation is required for this test. Follow collection instructions provided by the healthcare provider or laboratory.
SampleNasopharyngeal swab, Nasal wash swab, or Aspirate specimen collected in a special Viral transport medium (VTM). Confirm with the laboratory before booking.
MethodologyReal Time PCR, Cartridge-Based Nucleic Acid Amplification Test (CB-NAAT).
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of the virus at the time of sample collection. A negative result does not rule out infection, especially if exposure was recent or symptoms are mild. False negatives can occur. 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 Real-Time PCR technology, which is highly accurate for detecting the SARS-CoV-2 virus. However, like all tests, false negatives can occur.
Results are typically available the same day if the sample is received by 11 am. Confirm with the laboratory before booking.
A respiratory specimen, such as a nasopharyngeal swab or nasal wash swab, collected in a special Viral transport medium (VTM) is required.
A positive result indicates that the SARS-CoV-2 virus was detected in your sample. You should consult a healthcare professional for guidance.
A negative result suggests the virus was not detected at the time of testing. However, it does not completely rule out infection. Consult your doctor if you have concerns.
Yes, a convenient home sample collection service is available. Please inquire about availability and booking procedures.
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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