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Results: 81 to 99 of 99

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hermansky-Pudlak Syndrome & Pulmonary Fibrosis NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3640
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
123124
  • C Sequence analysis of the entire coding region

DYSKERATOSIS CONGENITA (AUTOSOMAL RECESSIVE)

Laboratorio de Genetica Clinica SL
Spain
56
  • C Sequence analysis of the entire coding region

Hereditary Hematopoietic Malignancy/Immunodeficiency Predisposition Panel

Genetic Services Laboratory University of Chicago
United States
7135
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dyskeratosis Congenita Panel

Blueprint Genetics
Finland
313
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary Immunodeficiency Panel

Blueprint Genetics
Finland
2275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Syndrome Panel

Blueprint Genetics
Finland
1122
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hematology Panel

Blueprint Genetics
Finland
4239
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone Marrow Failure

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
943
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
329127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone marrow failure syndromes Panel

CeGaT GmbH
Germany
1537
  • C Sequence analysis of the entire coding region

Dyskeratosis congenita Panel

CeGaT GmbH
Germany
810
  • C Sequence analysis of the entire coding region

Disorders associated with malignancy Panel

CeGaT GmbH
Germany
2645
  • C Sequence analysis of the entire coding region

NOP10 Single Gene

Fulgent Genetics
United States
11
  • 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

NOLA3 (NOP10) Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dyskeratosis Congenita NGS Panel

Fulgent Genetics
United States
148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dyskeratosis Congenita panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
1515
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Syndromes Panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
112116
  • C Sequence analysis of the entire coding region

Results: 81 to 99 of 99

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.