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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

PIK3CA - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Keratosis, seborrheic, somatic, 182000 (PIK3CA 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

Vascular malformations panel. 14-gene NGS panel.

Genologica Medica
Spain
3814
  • C Sequence analysis of the entire coding region

Lymphatic malformations and related disorders panel. NGS panel of 11 genes.

Genologica Medica
Spain
3111
  • C Sequence analysis of the entire coding region

Molecular profile of the breast tumor. Panel NGS genes: BRCA1, BRCA2, ERBB2, PIK3CA.

Genologica Medica
Spain
214
  • C Sequence analysis of the entire coding region

Macrocephaly / overgrowth syndrome panel. 43-gene NGS panel.

Genologica Medica
Spain
8843
  • C Sequence analysis of the entire coding region

Neuronal migration disorder panel. NGS panel of 58 genes.

Genologica Medica
Spain
11057
  • C Sequence analysis of the entire coding region

PIK3CA

Institute for Human Genetics University Medical Center Freiburg
Germany
131
  • C Sequence analysis of the entire coding region

Megalencephaly-Capillary Malformation Syndrome (PIK3CA Single Gene Test)

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuronal Migration Disorders NGS Panel

Fulgent Genetics
United States
39283
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Klippel-Trenaunay Syndrome (PIK3CA Single Gene Test)

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Macrocephaly/Overgrowth Syndrome NGS Panel

Fulgent Genetics
United States
10038
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
377114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PIK3CA Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • C Sequence analysis of the entire coding region

CLOVE syndrome, somatic (PIK3CA)

MVZ Dr. Eberhard & Partner Dortmund
Germany
101
  • E Sequence analysis of select exons

PIK3CA Single Gene

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

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.