U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

See more countries

Results: 21 to 40 of 71

Tests names and labsConditionsGenes, analytes, and microbesMethods

Dilated cardiomyopathy (WES based NGS panel of 81 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
181
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism (WES based NGS panel of 40 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
140
  • C Sequence analysis of the entire coding region

Hemochromatosis (WES based NGS panel of 8 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
18
  • C Sequence analysis of the entire coding region

Male Infertility Panel

CGC Genetics Unilabs
Portugal
1165
  • C Sequence analysis of the entire coding region

Female Infertility Panel

CGC Genetics Unilabs
Portugal
1129
  • C Sequence analysis of the entire coding region

Cardiovascular Comprehensive Panel 

CGC Genetics Unilabs
Portugal
1353
  • C Sequence analysis of the entire coding region

Cardiomyopathies Panel 

CGC Genetics Unilabs
Portugal
1197
  • C Sequence analysis of the entire coding region

Hematology Comprehensive Panel 

CGC Genetics Unilabs
Portugal
1291
  • C Sequence analysis of the entire coding region

Diabetes Panel

CGC Genetics Unilabs
Portugal
176
  • C Sequence analysis of the entire coding region

Hemochromatosis ( deletions/duplications in HFE, TFR2, HJV, HAMP and SLC40A1 genes)

CGC Genetics Unilabs
Portugal
15
  • D Deletion/duplication analysis

Hemochromatosis type 4 (sequence analysis of SLC40A1 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Hemochromatosis Panel

Mendelics
Brazil
16
  • C Sequence analysis of the entire coding region

MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES)

Laboratorio de Genetica Clinica SL
Spain
11372
  • E Sequence analysis of select exons

HEMOCHROMATOSIS HYPERFERRITINEMIA SYNDROME PANEL

Laboratorio de Genetica Clinica SL
Spain
18
  • E Sequence analysis of select exons

HYPERTROPHIC CARDIOMYOPATHY EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1197
  • E Sequence analysis of select exons

SUDDEN DEATH/ IDIOPATHIC VENTRICULAR FIBRILLATION EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1394
  • E Sequence analysis of select exons

DILATED CARDIOMYOPATHY EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1141
  • E Sequence analysis of select exons

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Hereditary hemochromatosis panel. Panel NGS genes: HAMP, HFE, HJV, SLC40A1, TFR2.

Genologica Medica
Spain
94
  • C Sequence analysis of the entire coding region

Hemochromatosis, type 4

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 71

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.