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Results: 61 to 80 of 88

Tests names and labsConditionsGenes, analytes, and microbesMethods

Prenatal Known Familial Mutation

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

NeoTYPE® Pancreas Tumor Profile

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
163
  • F Fluorescence in situ hybridization (FISH)
  • E Sequence analysis of select exons

NeoTYPE® Breast Tumor Profile

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
154
  • F Fluorescence in situ hybridization (FISH)
  • C Sequence analysis of the entire coding region

NeoTYPE® Ovarian Tumor Profile

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
158
  • F Fluorescence in situ hybridization (FISH)
  • C Sequence analysis of the entire coding region

NeoTYPE® Precision Profile for Solid Tumors

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
179
  • C Sequence analysis of the entire coding region

Custom XomeDxSlice (2-150 Genes, Proband Only)

GeneDx
United States
11718
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microcephaly Xpanded Panel

GeneDx
United States
1877
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paired Tumor/Normal - Solid Tumor Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2239
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paired Tumor/Normal - Comprehensive Solid Tumor Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2315
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
190
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Bone Marrow Failure (BMF)/Myelodysplastic Syndrome (MDS)/Leukemia Predisposition Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
4112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia NGS Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
825
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal disorders - different panels

Institute of Human Genetics Cologne University
Germany
875
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NewbornDx Advanced Sequencing Evaluation

Athena Diagnostics
United States
11722
  • C Sequence analysis of the entire coding region

Mirror movements: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Esophageal Atresia/Tracheoesophageal Fistula: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
524
  • C Sequence analysis of the entire coding region

Fanconi Anemia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2121
  • C Sequence analysis of the entire coding region

Caris MI TumorSeek Comprehensive Genomic Profile

Caris Life Sciences
United States
1591
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Familial Congenital Mirror Movements, Massive Sequencing (NGS) DCC, RAD51 Genes

Reference Laboratory Genetics
Spain
22
  • C Sequence analysis of the entire coding region

Mental retardation - different panels

Institute of Human Genetics Cologne University
Germany
72536
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 80 of 88

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.