Your Cart
Your cart is empty

Looks like you haven't added any test / checkup to your cart

Add Test / Checkup
User Sign In Health checkup offers
FISH for 6 Markers

FISH for 6 Markers

The Fluorescence In Situ Hybridization (FISH) for 6 Markers test is a valuable tool in the field of genetic analysis. This diagnostic test uses fluorescent probes to target and illuminate specific regions within the chromosomes, thereby allowing researchers and doctors to identify potential chromosomal abnormalities and gene alterations.

The FISH for 6 Markers test expands upon its counterparts by targeting six distinct chromosomal regions. This allows for a more comprehensive chromosomal analysis, proving particularly useful in complex medical scenarios, such as diagnosing and monitoring cancer or understanding congenital disabilities.


  • Test NameFISH for 6 Markers
  • Sample TypeTissue or Cells
  • Preparations RequiredNo specific patient preparation is required for this test. However, it is essential to follow the instructions given by your doctor regarding the sample collection procedure.
  • Report Time5 days

What is the FISH for 6 Markers test?

FISH for 6 Markers is a genetic diagnostic test that uses fluorescent probes to highlight six distinct chromosomal regions. This helps detect chromosomal abnormalities or gene alterations, useful for diagnosing, monitoring, and treating various diseases.

Why is this test done?

This test is often used in diagnosing and monitoring cancers, as the identification of genetic abnormalities can help determine the best treatment options. It is also utilized in genetic counseling and the diagnosis of other genetic disorders.

Home Sample Collection Process

1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
Download Reports
Download Reports
Frequently Asked Questions

The test requires a tissue or cell sample. The sample is treated with fluorescent probes that bind to the specific chromosomal regions of interest. When viewed under a fluorescence microscope, these regions glow, highlighting any potential abnormalities.

The presence or absence of fluorescence signals at the targeted chromosomal regions can indicate genetic or chromosomal abnormalities. However, interpretation of these results should be done by a qualified professional in conjunction with other clinical and diagnostic information.

The test results are usually available within 7 to 14 days. However, this timeframe may vary depending on the laboratory performing the test.

The risks of this test are primarily related to the sample collection procedure and can include discomfort, bleeding, or potential infection. The FISH test itself does not pose any risk to the patient.

The results can provide critical information about the genetic aspects of a disease, which can guide treatment choices, disease management, and prognosis.

No, fasting is not necessary for this test.

No specific preparation is required. However, patients should follow any instructions provided by their doctor regarding the sample collection procedure.

If the test results indicate abnormalities, you should consult a geneticist or an oncologist, particularly if the test was done in relation to cancer diagnosis.

The test results can be influenced by factors such as the quality of the sample and the laboratory techniques employed.

Medications typically do not affect the genetic features of cells and are unlikely to influence the results of this test.

The FISH for 6 Markers test is widely available, but accessibility may vary depending on the region and the healthcare system.

The frequency of the test depends on the clinical scenario and should be determined by your doctor based on your health condition and medical history.

Yes, there are alternative genetic tests such as karyotyping and comparative genomic hybridization (CGH) which can also be used for chromosomal analysis.

The FISH for 6 Markers test is an essential diagnostic tool that offers in-depth insights into one's chromosomal makeup. This test is particularly valuable in understanding and managing complex diseases like cancer, where genetic abnormalities play a significant role. It is important to discuss your test results with your doctor for appropriate guidance and treatment planning. Early detection and understanding of chromosomal abnormalities can make a significant difference in disease outcomes and management strategies.

FISH for 6 markers
₹ 20000
Schedule Test in Your Available Time
Locations Near You in Hyderabad
  • 4KM from Madhapur
  • 3KM from Banjara Hills
  • 1.9KM from Yusufguda
  • 3KM from Madhura Nagar
  • 5KM from Shaikpet