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Results: 41 to 60 of 99

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Cancer Panel

Mendelics
Brazil
137
  • C Sequence analysis of the entire coding region

Endocrine Neoplasia Panel

Mendelics
Brazil
141
  • C Sequence analysis of the entire coding region

Hereditary Anemias Panel

Mendelics
Brazil
1183
  • C Sequence analysis of the entire coding region

Hereditary Breast Cancer and Ovarian Cancer

Mendelics
Brazil
137
  • C Sequence analysis of the entire coding region

Hereditary Cancer Panel (Complete)

Mendelics
Brazil
1264
  • C Sequence analysis of the entire coding region

Prostate Cancer Panel (HRR)

Mendelics
Brazil
140
  • C Sequence analysis of the entire coding region

Immunodeficiencies and Immunologic Diseases Panel (Complete)

Mendelics
Brazil
1397
  • C Sequence analysis of the entire coding region

Male Infertility Panel

Mendelics
Brazil
137
  • C Sequence analysis of the entire coding region

HEREDITARY CANCER EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1249
  • E Sequence analysis of select exons

BREAST AND OVARIAN CANCER EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
148
  • E Sequence analysis of select exons

SKELETAL DYSPLASIAS PANEL

Laboratorio de Genetica Clinica SL
Spain
1643
  • E Sequence analysis of select exons

BONE MARROW FAILURE SYNDROME PANEL

Laboratorio de Genetica Clinica SL
Spain
1165
  • E Sequence analysis of select exons

HEREDITARY ANEMIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1144
  • E Sequence analysis of select exons

FANCONI ANEMIA EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
126
  • E Sequence analysis of select exons

Limb malformation panel. NGS panel of 45 genes.

Genologica Medica
Spain
7745
  • C Sequence analysis of the entire coding region

Bone marrow failure syndrome panel. NGS panel of 122 genes.

Genologica Medica
Spain
194122
  • C Sequence analysis of the entire coding region

Fanconi anemia panel

Genologica Medica
Spain
3522
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel (66 Genes)

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
3566
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prenatal Known Familial Mutation

GeneDx
United States
11716
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Results: 41 to 60 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.