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Results: 21 to 38 of 38

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Chromosomal Microarray Analysis

Invitae
United States
6225
  • D Deletion/duplication analysis

Invitae NIPS for Singleton Pregnancies (chromosomes 13, 18, 21)

Invitae
United States
1111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae NIPS for Twin Pregnancies (chromosomes 13, 18, 21)

Invitae
United States
33
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Karyotype from Blood

Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS
India
151
  • K Karyotyping

Multiplex Trisomy/Sex Chromosome Screen

Genetics Laboratory Shodair Children's Hospital
United States
45
  • U Uniparental disomy study (UPD)

Non-invasive Prenatal Screen with Microdeletions

PathGroup
United States
1110
  • T Targeted variant analysis

MaterniT GENOME

Integrated Genetics – Sequenom
United States
231
  • T Targeted variant analysis

Chromosome Analysis with Reflex to Genomic Microarray

ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories
United States
161
  • K Karyotyping
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Prequel Prenatal Screen

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

Panoroma Non-invasive Prenatal Test

LifeLabs Genetics
Canada
44
  • T Targeted variant analysis

Prenatal Rapid Screen by FISH for 13, 16, 18, 21, X and Y

Center for Comprehensive Genetic Services Shahid Beheshti University of Medical Sciences
Iran
56
  • I FISH-interphase
  • M FISH-metaphase
  • K Karyotyping

Chromosome Analysis: Karyotype

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

180K CGH+SNP microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
2311
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Prenatal Rapid Screen by FISH for 13, 16, 18, 21, X and Y

Genomic Research Center Shahid Beheshti University of Medical Sciences
Iran
56
  • I FISH-interphase
  • M FISH-metaphase
  • K Karyotyping

Karyotyping / Chromosome Rearrangements with Abnormal Phenotypes

MGZ Medical Genetics Center
Germany
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

Cytogenomic SNP Microarray

ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories
United States
161
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Results: 21 to 38 of 38

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.