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Results: 21 to 32 of 32

Tests names and labsConditionsGenes, analytes, and microbesMethods

Macrocephaly/Overgrowth Syndrome NGS Panel

Fulgent Genetics
United States
10038
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PERLMAN SYNDROME

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Invitae Overgrowth and Macrocephaly Syndromes Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
4320
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Pediatric Solid Tumors Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
9048
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Wilms Tumor Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal / Urinary Cancer Comprehensive Panel

Fulgent Genetics
United States
7327
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
329127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
134139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Renal/Urinary Tract Cancers Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
3724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
13880
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DIS3L2 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
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 32 of 32

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.