Genetic Testing Menu

 

Insight Medical Genetics is home to a full-service CLIA-licensed and CAP certified cytogenetic and molecular genetics laboratories. Highly trained lab technologists provide in-house testing for a wide range of diagnostic and screening tests with particular capacities to handle and process prenatal samples. Insight can provide lab services to providers nationwide and internationally. 

 

Below is a complete list of Insight's lab capabilities. Custom requests are accepted on a case-by-case basis after review by lab team. For a complete gene list, click here

TestWhen To OrderTurnaround Time Prenatal Carrier Screening/
Adult
Chromosome Analysis (Karyotype) Routine Screening
Advanced Maternal Age
Ultrasound Anomalies
Family History
Less than 14 days
FISH (13, 18, 21, X, Y)Routine Screening
Advanced Maternal Age
Ultrasound Anomalies
Family History
1 business day
Chromosomal Microarray (aCGH)Routine Screening
Advanced Maternal Age
Ultrasound Anomalies
Family History
10-21 days (direct)
16-28 days (culture)
Skeletal Dysplasia/ Osteogenesis
Imperfecta NGS Panel (33 genes)
Fractures
Short long bones
Family History
Prenatal Diagnosis
2-4 weeks
Noonan Syndrome
NGS Panel (12 genes)
Increased Nuchal Translucency
Prenatal Diagnosis
Family History
2-4 weeks
Sanger Sequencing:
Full gene and targeted
(SMN1, GBA, CFTR, and more...)
Carrier Screening
Prenatal Diagnosis
Reflex Sequencing
Family History
1-3 weeks
SMN1 Deletion/Duplication Analysis Carrier Screening
Prenatal Diagnosis
Reflex Testing
Family History
1-2 weeks
FMR1 CGG Repeat and
Methylation Analysis
Carrier Screening
Prenatal Diagnosis
Family History
1-3 weeks
HBA1/HBA2 Deletion/Duplication
Analysis
Carrier Screening
Prenatal Diagnosis
Reflex Testing
Family History
2-3 weeks
Custom Sanger Sequencing:
Full gene and targeted
Carrier Screening
Prenatal Diagnosis
Reflex Sequencing
Family History
3-5 weeks
Maternal Cell Contamination Recommended as complement to all prenatal testing With respective test