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Results: 1 to 20 of 13188

Tests names and labsConditionsGenes, analytes, and microbesMethods

Psychotropic Pharmacogenomics Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
122
  • T Targeted variant analysis

NGS Panel for Hemochromatosis and Hyperferritinemia /Hypoferritinemia Panel

BloodGenetics
Spain
1111
  • C Sequence analysis of the entire coding region

Cerebral cavernous malformation panel. Panel NGS genes: CCM2, KRIT1, PDCD10, RASA1.

Genologica Medica
Spain
54
  • C Sequence analysis of the entire coding region

Leukodystrophy and leukoencephalopathy panel. NGS panel of 74 genes.

Genologica Medica
Spain
9674
  • C Sequence analysis of the entire coding region

Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes.

Genologica Medica
Spain
4221
  • C Sequence analysis of the entire coding region

Hyperammonemia and urea cycle disorders panel. 48-gene NGS panel.

Genologica Medica
Spain
4948
  • C Sequence analysis of the entire coding region

Lymphatic malformations and related disorders panel. NGS panel of 11 genes.

Genologica Medica
Spain
3111
  • C Sequence analysis of the entire coding region

Periodic paralysis panel. Panel NGS genes: CACNA1S, CLCN1, KCNJ2, SCN4A.

Genologica Medica
Spain
134
  • C Sequence analysis of the entire coding region

Congenital structural heart disease panel. NGS panel of 62 genes.

Genologica Medica
Spain
11362
  • C Sequence analysis of the entire coding region

Panel of exostoses and related disorders. Panel NGS genes: EXT1, EXT2, PTPN11.

Genologica Medica
Spain
83
  • C Sequence analysis of the entire coding region

Branchial-Oto-Renal Syndrome Panel. Panel NGS genes: EYA1, SIX1, SIX5, TFAP2A.

Genologica Medica
Spain
74
  • C Sequence analysis of the entire coding region

Metabolic myopathy and rhabdomyolysis panel. NGS panel of 52 genes.

Genologica Medica
Spain
8952
  • C Sequence analysis of the entire coding region

Congenital and familial lipodystrophy panel. NGS panel of 11 genes.

Genologica Medica
Spain
2911
  • C Sequence analysis of the entire coding region

Hyperphenylalaninemia panel. Panel NGS genes: GCH1, PAH, PCBD1, PTS, QDPR.

Genologica Medica
Spain
65
  • C Sequence analysis of the entire coding region

Panel of disorders related to collagen type VI. 6-gene NGS panel.

Genologica Medica
Spain
116
  • C Sequence analysis of the entire coding region

Hereditary hemochromatosis panel. Panel NGS genes: HAMP, HFE, HJV, SLC40A1, TFR2.

Genologica Medica
Spain
94
  • C Sequence analysis of the entire coding region

Hereditary lung cancer panel. Panel NGS genes: BRCA2, CDKN2A, EGFR, TP53.

Genologica Medica
Spain
234
  • C Sequence analysis of the entire coding region

Panel of facial dysostosis and related disorders. NGS panel of 26 genes.

Genologica Medica
Spain
3526
  • C Sequence analysis of the entire coding region

Septo-optic dysplasia panel. Panel NGS genes: HESX1, OTX2, PAX6, SOX2.

Genologica Medica
Spain
114
  • C Sequence analysis of the entire coding region

Renal tubular acidosis panel. Panel NGS genes: ATP6V0A4, ATP6V1B1, CA2, SLC4A1, SLC4A4.

Genologica Medica
Spain
155
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 13188

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.