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34 labs with tests matching your search, 4 labs matching in other ways
Lab name Tests matching your search
ARUP Laboratories, Molecular Genetics and Genomics United States1
Amsterdam UMC Genome Diagnostics Netherlands8
Athena Diagnostics United States2
Bioarray Spain9
Blueprint Genetics Finland2
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada2
CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany1
CGC Genetics Portugal6
CeGaT GmbH Germany13
DDC Clinic Molecular Diagnostics Laboratory United States2
DNA Labs India India7
Dhiti Omics Technologies Private Ltd India1
Dubai Health Genomic Medicine Center United Arab Emirates1
Fulgent Genetics United States24
GeneDx United States1
Genesys Diagnostics United States1
Genetic Services Laboratory United States1
Genome Diagnostics Laboratory Canada2
Genome Diagnostics Laboratory Netherlands1
Integrated Genetics Westborough United States8
Intergen Genetics and Rare Diseases Diagnosis Center Turkey25
Johns Hopkins Genomics DNA Diagnostic Laboratory United States1
Labcorp Genetics (formerly Invitae) United States11
MGZ Medical Genetics Center Germany2
MNG Laboratories (Medical Neurogenetics, LLC.) United States1
Machaon Diagnostics United States1
Mayo Clinic Laboratories United States5
Molecular Vision Laboratory United States2
Myriad Genetics, Inc. United States1
Natera, Inc. United States4
Praxis fuer Humangenetik Wien Austria1
PreventionGenetics, part of Exact Sciences United States7
Revvity Omics United States1
Secugen SL Spain1
Breakthrough Genomics United States0
Breda Genetics srl Italy0
Dasa Brazil0
Victorian Clinical Genetics Services Australia0
Results:
156 genetic tests from 34 labs with tests matching your search, 4 labs matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Aicardi-Goutieres syndrome 7, 615846, Autosomal dominant; AGS7 (Aicardi-Goutières syndrome) (IFIH1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 1, dominant and recessive, 225750, Autosomal recessive, Autosomal dominant; AGS1 (Aicardi-Goutières syndrome) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 5, 612952, Autosomal recessive; AGS5 (Aicardi-Goutières syndrome) (Prenatal) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 5, 612952, Autosomal recessive; AGS5 (Aicardi-Goutières syndrome) (SAMHD1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 7, 615846, Autosomal dominant; AGS7 (Aicardi-Goutières syndrome) (IFIH1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 2, 610181, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (RNASEH2B gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (RNASEH2A gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 2, 610181, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (RNASEH2B gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (RNASEH2A gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 3, 610329, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (Prenatal) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 2, 610181, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 1, dominant and recessive, 225750, Autosomal recessive, Autosomal dominant; AGS1 (Aicardi-Goutières syndrome) (TREX1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 5, 612952, Autosomal recessive; AGS5 (Aicardi-Goutières syndrome) (SAMHD1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 3, 610329, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (RNASEH2C gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 6, 615010, Autosomal recessive; AGS6 (Aicardi-Goutières syndrome) (ADAR gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 6, 615010, Autosomal recessive; AGS6 (Aicardi-Goutières syndrome) (ADAR gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 1, dominant and recessive, 225750, Autosomal recessive, Autosomal dominant; AGS1 (Aicardi-Goutières syndrome) (Prenatal) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Aicardi-Goutieres syndrome 3, 610329, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (Prenatal) (MLPA)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis
156 tests from 34 labs
See all labs
View the list of labs matching your search query.
More help
❮Page 1 of 8❯
Aicardi-Goutieres syndrome 7, 615846, Autosomal dominant; AGS7 (Aicardi-Goutières syndrome) (IFIH1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 1, dominant and recessive, 225750, Autosomal recessive, Autosomal dominant; AGS1 (Aicardi-Goutières syndrome) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 5, 612952, Autosomal recessive; AGS5 (Aicardi-Goutières syndrome) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 5, 612952, Autosomal recessive; AGS5 (Aicardi-Goutières syndrome) (SAMHD1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 7, 615846, Autosomal dominant; AGS7 (Aicardi-Goutières syndrome) (IFIH1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 2, 610181, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (RNASEH2B gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (RNASEH2A gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 2, 610181, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (RNASEH2B gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (RNASEH2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 3, 610329, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 4, 610333, Autosomal recessive; AGS4 (Aicardi-Goutières syndrome) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 2, 610181, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 1, dominant and recessive, 225750, Autosomal recessive, Autosomal dominant; AGS1 (Aicardi-Goutières syndrome) (TREX1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 5, 612952, Autosomal recessive; AGS5 (Aicardi-Goutières syndrome) (SAMHD1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 3, 610329, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (RNASEH2C gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 6, 615010, Autosomal recessive; AGS6 (Aicardi-Goutières syndrome) (ADAR gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 6, 615010, Autosomal recessive; AGS6 (Aicardi-Goutières syndrome) (ADAR gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 1, dominant and recessive, 225750, Autosomal recessive, Autosomal dominant; AGS1 (Aicardi-Goutières syndrome) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Aicardi-Goutieres syndrome 3, 610329, Autosomal recessive; AGS2 (Aicardi-Goutières syndrome) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. 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.