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CVS Karyotyping + FISH 13/18/21/X/Y
CVS Karyotyping + FISH 13/18/21/X/Y
Karyotyping is a test performed on Chorionic Villi Sample (CVS) to identify fetal chromosomal numerical abnormalities (aneuploidy) and structural rearrangements such as inversions, insertions, translocations etc in the fetus. FISH 13/18/21/X/Y is ordered in addition for a quick result to confirm or rule out only Trisomy 13 (Patau Syndrome), 18 (Edward syndrome), 21 (Down Syndrome), and Sex chromosomal aneuploidy.
14000
₹2599
76% OFF
2 weeks
Schedule test now
Schedule test now
Sample Collection and Transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
CVS Karyotyping + FISH 13/18/21/X/Y; CVS chromosomal analysis + FISH 13/18/21
Specialities
ObGyn, IVF, Fetal Medicine
Technology
CVS Karyotyping: Cells from chorionic villus sample are cultured and mitotic (dividing) cells are examined under microscope followed by automated image analysis for karyotyping (systematic arrangement of chromosomes). A minimum of 25 cells are scored under microscope and 5 cells Karyotyped to identify chromosomal abnormalities including numerical defects (aneuploidy) or structural changes such a balanced translocations, inversions, insertions etc along with mosaicism. The testdoes not detect small copy number variations or DNA variants. FISH: DNA probes (small molecules of DNA that are designed to hybridise with a particular section of the genome) are used detect specific complementary sequences on a chromosome. It is undertaken in situ on chromosomes spread on a slide and visualised by microscopy.
Conditions & Symptoms
High risk screening (Double marker or NIPT) results, high risk for aneuploidy, bad obstetric history, parents carriers of translocations, history of baby or fetus with Trisomy 13 (Patau Syndrome), Trisomy 18 (Edward Syndrome) or Trisomy 21 (Down Syndrome), Turner Syndrome (XO), Klienefleter Syndrome (XYY) or Triple X Syndrome (XXX), ultrasound markers
Additional Information
GeneTech pioneered genetic testing in India in 1998 and has the most comprehensive range of tests using technologies.
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Enhancing IVF Outcomes: GeneAndro and GeneFemina Explained
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Achieving IVF Success: Insights on GeneAndro and GeneFemina
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Karyotyping is a test performed on Chorionic Villi Sample (CVS) to identify fetal chromosomal numerical abnormalities (aneuploidy) and structural rearrangements such as inversions, insertions, translocations etc in the fetus.
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Test CatalogueCVS Karyotyping + FISH 13/18/21/X/Y

Full Body Checkup - Essential in Hyderabad

Unlock insights into your health, ancestry, or future risks with our advanced genetic testing. Backed by cutting-edge science and expert guidance, Genetech helps you make informed decisions—personalized to your DNA.

₹1599
₹2599
76% OFF
2 weeks
Schedule test now

CVS Karyotyping + FISH 13/18/21/X/Y

Karyotyping is a test performed on Chorionic Villi Sample (CVS) to identify fetal chromosomal numerical abnormalities (aneuploidy) and structural rearrangements such as inversions, insertions, translocations etc in the fetus. FISH 13/18/21/X/Y is ordered in addition for a quick result to confirm or rule out only Trisomy 13 (Patau Syndrome), 18 (Edward syndrome), 21 (Down Syndrome), and Sex chromosomal aneuploidy.

14000
₹2599
76% OFF
3 weeks + 3 days
Schedule test now
Sample collection and transportation
Sample Collection: 3ml Peripheral Blood in PURPLE TOP (EDTA) Vacutainer Transport within 48 hrs at room temperature
Download Brochure
Alternate Names
CVS Karyotyping + FISH 13/18/21/X/Y; CVS chromosomal analysis + FISH 13/18/21
Specialities
ObGyn, IVF, Fetal Medicine
Technology
CVS Karyotyping: Cells from chorionic villus sample are cultured and mitotic (dividing) cells are examined under microscope followed by automated image analysis for karyotyping (systematic arrangement of chromosomes). A minimum of 25 cells are scored under microscope and 5 cells Karyotyped to identify chromosomal abnormalities including numerical defects (aneuploidy) or structural changes such a balanced translocations, inversions, insertions etc along with mosaicism. The testdoes not detect small copy number variations or DNA variants. FISH: DNA probes (small molecules of DNA that are designed to hybridise with a particular section of the genome) are used detect specific complementary sequences on a chromosome. It is undertaken in situ on chromosomes spread on a slide and visualised by microscopy.
Conditions & Symptoms
High risk screening (Double marker or NIPT) results, high risk for aneuploidy, bad obstetric history, parents carriers of translocations, history of baby or fetus with Trisomy 13 (Patau Syndrome), Trisomy 18 (Edward Syndrome) or Trisomy 21 (Down Syndrome), Turner Syndrome (XO), Klienefleter Syndrome (XYY) or Triple X Syndrome (XXX), ultrasound markers
Related Tests
Genetic Counselling
Our genetic counselling services empower patients and families by providing expert guidance on genetic conditions, their risks, and inheritance patterns. Our counsellors assess family medical histories to identify potential genetic risks and explain the benefits and limitations of genetic testing.
750
2 weeks
Book now
Amniocentesis
Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy. Amniocentesis is an ultrasound guided sterile proceedure performed by experienced radiologits to retrive 20-30ml of the amniotic fluid from the womb. The fluid which contains fetal cells is used in the genetic lab to test for genetic abnormalities. It is done between 16-22 weeks of gestation. Amniocentesis proceedure is done at our central laboratory in Hyderabad. Prior appointment required. Call 9848041127 for details
7500
2 weeks
Book now
CVS Karyotyping
Karyotyping is a test performed on Chorionic Villi Sample (CVS) to identify fetal chromosomal numerical abnormalities (aneuploidy) and structural rearrangements such as inversions, insertions, translocations etc in the fetus.
8000
2 weeks
Book now

Frequently asked questions

What is Genetic Testing?
What are the uses of Genetic Testing?
What are the types of Genetic testing?
Are all genetic disorders hereditary?
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GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.
GeneTech can provide online or offline counseling to patients in various languages. Some counseling sessions may require presence of a junior or on-duty physician for local language assistance.
Book counseling in advance. The date and time requested on this form are not confirmed until our Service Coordinator calls you to inform the appointment date and time, and payment for counseling is done.
Call +91-98480-41127 for any additional information or directions to pour branches or head-office.

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