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Results: 1 to 20 of 29773

Tests names and labsConditionsGenes, analytes, and microbesMethods

Genomic Unity® 2.0 - comparator

Variantyx, Inc.
United States
11
  • C Sequence analysis of the entire coding region

Genomic Unity® 2.0 - singleton

Variantyx, Inc.
United States
11
  • C Sequence analysis of the entire coding region

Genomic Unity® Hearing Loss Disorders Analysis

Variantyx, Inc.
United States
1318
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

IriSight™ CNV Analysis

Variantyx, Inc.
United States
22
  • D Deletion/duplication analysis

Genomic Unity® Nuclear Encoded Mitochondrial Gene Analysis

Variantyx, Inc.
United States
1335
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity® Mitochondrial Genome Deletions Analysis

Variantyx, Inc.
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OncoAlly™ Hereditary Colorectal Cancer Analysis

Variantyx, Inc.
United States
121
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

OncoAlly™ Common Hereditary Cancers Analysis

Variantyx, Inc.
United States
146
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

OncoAlly™ Comprehensive Hereditary Cancer Analysis

Variantyx, Inc.
United States
188
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

OncoAlly™ BRCA1/2 Analysis Analysis

Variantyx, Inc.
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genomic Unity® Genome-wide CNV and FMR1 Analysis

Variantyx, Inc.
United States
52
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity® Dementia Analysis

Variantyx, Inc.
United States
632
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

IriSight® Comprehensive Analysis - Prenatal Proband

Variantyx, Inc.
United States
12
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity Exome Analysis - Proband (includes STR analysis of 36 loci)

Variantyx, Inc.
United States
11
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity Mitochondrial Genome Analysis

Variantyx, Inc.
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

T-cell acute lymphoblastic leukemia, somatic, 613065 (Acute lymphoblastic leukemia) (BAX gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Brachydactyly, type B2, 611377, Autosomal dominant; BDB2 (Brachydactyly type B2) (NOG gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Asthma, susceptibility to, 600807, Autosomal dominant (SCGB3A2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Anorexia nervosa, susceptibility to, 606788 (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Basal cell nevus syndrome, 109400, Autosomal dominant (Gorlin syndrome) (Prenatal) (MLPA)

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

Results: 1 to 20 of 29773

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.