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Results: 41 to 58 of 58

Tests names and labsConditionsGenes, analytes, and microbesMethods

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation, Panel Massive Sequencing (NGS) 30 Genes

Reference Laboratory Genetics
Spain
3030
  • C Sequence analysis of the entire coding region

CONGENITAL DISORDERS OF GLYCOSYLATION

Laboratorio de Genetica Clinica SL
Spain
55
  • C Sequence analysis of the entire coding region

Congenital Disorder of Glycosylation Type IC , Sequencing ALG6 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital disorder of glycosylation type Ic

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing ALG6

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
173204
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation (CDG)

MGZ Medical Genetics Center
Germany
438
  • C Sequence analysis of the entire coding region

ALG6 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperinsulinism NGS Panel

Fulgent Genetics
United States
4121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation NGS Panel

Fulgent Genetics
United States
4339
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 58 of 58

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.