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Results: 21 to 35 of 35

Tests names and labsConditionsGenes, analytes, and microbesMethods

Non-invasive Prenatal Screen with Microdeletions

PathGroup
United States
1110
  • T Targeted variant analysis

Prequel Prenatal Screen

Myriad Genetics, Inc.
United States
1310
  • C Sequence analysis of the entire coding region

Chromosome Analysis: Karyotype

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
201
  • K Karyotyping

Male Factor Infertility

Asper Biogene Asper Biogene LLC
Estonia
9990
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

FISH, SRY/X Centromere

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
51
  • M FISH-metaphase

Chromosome Analysis, Tissue

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
61
  • K Karyotyping

Chromosome Analysis, Mosaicism

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
101
  • K Karyotyping

Chromosome Analysis, High Resolution

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
91
  • K Karyotyping

Chromosome Analysis, Blood

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
91
  • K Karyotyping

Chromosome Analysis, Tissue

Quest Diagnostics Nichols Institute Chantilly
United States
91
  • K Karyotyping

Chromosome Analysis, Mosaicism

Quest Diagnostics Nichols Institute Chantilly
United States
91
  • K Karyotyping

Chromosome Analysis, Blood

Quest Diagnostics Nichols Institute Chantilly
United States
91
  • K Karyotyping

MaterniT21

Integrated Genetics – Sequenom
United States
1211
  • T Targeted variant analysis

Chromosome analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
71
  • K Karyotyping

Chromosome analysis

ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories
United States
146
  • K Karyotyping

Results: 21 to 35 of 35

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.