Genomic translocation analysis (embryo)
This test examines the genetic material of your embryo to check for structural changes in chromosomes that may affect its health or development.
["Helps identify potential genetic risks before implantation for personalized reproductive planning."]
Key facts at a glance
- LOINC
- 101395-2
- Short code
- Translocation analysis Embryo
- Synonyms
- Translocation analysis Embryo
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- CPT
- 86038
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
A translocation is a genetic rearrangement where parts of chromosomes swap places. This test detects such rearrangements in the embryo’s DNA, which can sometimes lead to developmental issues or increased risk of miscarriage.
Why It’s Done
Doctors may recommend this test if you’re undergoing in vitro fertilization (IVF) and have a history of recurrent miscarriages, infertility, or a family history of genetic disorders. It helps ensure the embryo has a normal genetic makeup before being implanted in your uterus.
Sample Collection and Process
A small sample of your embryo is collected during IVF, typically after fertilization. The DNA is extracted and analyzed for chromosomal abnormalities, often using advanced genetic sequencing techniques.
Preparation and Timeline
No special preparation is needed before the test. Results are usually available within a few days to a week, depending on the laboratory’s processing time.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test plays a critical role in reproductive medicine by providing critical information about an embryo’s genetic health. Translocations can sometimes cause genetic disorders, developmental delays, or increased risks of pregnancy complications. By identifying these issues early, healthcare providers can guide decisions about embryo selection, potentially improving the chances of a healthy pregnancy.
Short name
Embryo Genetic Screening for Chromosomal Abnormalities
Frequently asked questions
Will this test affect my ability to have more children in the future?
How much does this test cost, and is it covered by insurance?
What if the test shows an abnormality in the embryo?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy