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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Osteofibrous dysplasia, susceptibility to, 607278, Autosomal dominant (MET 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

Osteofibrous dysplasia, susceptibility to, 607278, Autosomal dominant (MLPA)

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

Paternity DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

CentoCancer

Centogene AG - the Rare Disease Company
Germany
11368
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoCancer Comprehensive

Centogene AG - the Rare Disease Company
Germany
155107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Solid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
218135
  • C Sequence analysis of the entire coding region

MET - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Deafness Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
405219
  • D Deletion/duplication analysis

Invitae Genetic Health Screen

Labcorp Genetics (formerly Invitae) LabCorp
United States
409164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cancer Screen

Labcorp Genetics (formerly Invitae) LabCorp
United States
16062
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Hearing Loss and Deafness Panel

PreventionGenetics, part of Exact Sciences
United States
361224
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Inherited Cancer Panel

Dhiti Omics Technologies Private Ltd
India
13584
  • C Sequence analysis of the entire coding region

Detection of MET amplification in gastric cancer

Genologica Medica
Spain
41
  • C Sequence analysis of the entire coding region

Non-syndromic hearing loss panel. 95-gene NGS panel.

Genologica Medica
Spain
14694
  • C Sequence analysis of the entire coding region

Hereditary endocrine cancer panel. NGS panel of 22 genes.

Genologica Medica
Spain
6822
  • C Sequence analysis of the entire coding region

Hereditary kidney cancer panel. NGS panel of 26 genes.

Genologica Medica
Spain
7426
  • C Sequence analysis of the entire coding region

MET

Institute for Human Genetics University Medical Center Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Baylor Genetics
United States
13261
  • E Sequence analysis of select exons

Hereditary Renal Cancer Panel

Baylor Genetics
United States
4113
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary onco-endocrino tumors (50 genes)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
2549
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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