| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|
Sacral agenesis with vertebral anomalies, 615709, Autosomal recessive; SAVA (Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome) (T gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Sacral agenesis with vertebral anomalies, 615709, Autosomal recessive; SAVA (Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome) (T gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Neural tube defects, susceptibility to, 182940, Autosomal dominant (Neural tube closure defect) (T gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Oncological diseases panel _v.2.0 CGC Genetics Unilabs
Portugal | 1 | 205 | - C Sequence analysis of the entire coding region
|
Genomic Unity® Custom Analysis Variantyx, Inc.
United States | 1 | 4054 | - D Deletion/duplication analysis
- X Mutation scanning of select exons
- C Sequence analysis of the entire coding region
|
TBXT Single Gene Fulgent Genetics
United States | 1 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Clinical Exome Fulgent Genetics
United States | 5128 | 4672 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
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NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute
for medical advice. Patients and consumers with specific questions
about a genetic test should contact a health care provider or a genetics professional.
