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Results: 1 to 20 of 25

Tests names and labsConditionsGenes, analytes, and microbesMethods

IRF6 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Polydactyly and Syndactyly Panel

PreventionGenetics, Part of Exact Sciences
United States
320231
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Orofacial cleft 6, 608864, Isolated cases; OFC6 (Cleft lip/palate) (Prenatal) (MLPA)

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

Orofacial cleft 6, 608864, Isolated cases; OFC6 (Cleft lip/palate) (MLPA)

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

Orofacial cleft 6, 608864, Isolated cases; OFC6 (Cleft lip/palate) (IRF6 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Orofacial cleft 6, 608864, Isolated cases; OFC6 (Cleft lip/palate) (IRF6 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Van der Woude Syndrome Panel

PreventionGenetics, Part of Exact Sciences
United States
42
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cleft Lip/Cleft Palate Panel

PreventionGenetics, Part of Exact Sciences
United States
177163
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Ectodermal Dysplasia and Related Disorders Panel

Invitae
United States
14873
  • D Deletion/duplication analysis

IRF6

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

Cleft lip panel, cleft palate and associated syndromes. 16-gene NGS panel.

Genologica Medica
Spain
4916
  • C Sequence analysis of the entire coding region

Kabuki syndrome panel. 7-gene NGS panel.

Genologica Medica
Spain
167
  • C Sequence analysis of the entire coding region

Genital Abnormalities / Sex Development Disorders Panel

Genologica Medica
Spain
9549
  • C Sequence analysis of the entire coding region

Skeletal diseases. NGS panel of 169 genes.

Genologica Medica
Spain
373169
  • C Sequence analysis of the entire coding region

Orofacial cleft: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
87
  • C Sequence analysis of the entire coding region

Popliteal Pterygium Syndrome (IRF6 Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cleft Palate/Lip NGS Panel

Fulgent Genetics
United States
12723
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kabuki Syndrome NGS Panel

Fulgent Genetics
United States
177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Van der Woude Syndrome NGS Panel

Fulgent Genetics
United States
122
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing IRF6

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 25

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.