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Results: 21 to 40 of 44

Tests names and labsConditionsGenes, analytes, and microbesMethods

Chromosome 1p36 deletion syndrome, 607872, Isolated cases (1p36 deletion syndrome) (Prenatal) (440)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Chromosome 1p36 deletion syndrome, 607872, Isolated cases (1p36 deletion syndrome) (440)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

qChip 180

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • 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

1p36 deletion syndrome

Genetics Service Unit National Institute of Biomedical Genomics
India
11
  • D Deletion/duplication analysis

QNatal Advanced

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
1513
  • C Sequence analysis of the entire coding region

Constitutional Chromosomal Microarray Analysis

Clinical Genomics Laboratory Laboratory for Precision Diagnostics, University of Washington
United States
261
  • D Deletion/duplication analysis

Microarray Testing

Cytogenetics Laboratory SUNY Upstate Medical University
United States
1141
  • F Fluorescence in situ hybridization (FISH)

Detection by FISH of 1p3 6 deletion

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

NIPT extended

CIBIC S.A.
Argentina
1112
  • D Deletion/duplication analysis

NIPT in POC

CIBIC S.A.
Argentina
1112
  • D Deletion/duplication analysis

NIPT Basic

CIBIC S.A.
Argentina
114
  • D Deletion/duplication analysis

NIPT Singleton

Ambry Genetics
United States
109
  • D Deletion/duplication analysis

FISH Follow-up

GeneDx
United States
131
  • M FISH-metaphase

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

Prequel Prenatal Screen

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

Frequent syndromes panel

Genolife Información de Vida
Mexico
67
  • D Deletion/duplication analysis

1p36 Deletion Syndrome

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
11
  • I FISH-interphase
  • M FISH-metaphase

Panoroma Non-invasive Prenatal Test

LifeLabs Genetics
Canada
66
  • T Targeted variant analysis

Results: 21 to 40 of 44

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.