Clinical and research tests for 3358 - Genetic Testing Registry (GTR)

Results: 1 to 16 of 16

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
SmartMeds+ Pharmacogenomic Testing By Innovative GX Health Innovative Genomics InnovativeGx Health United States	1	67	T Targeted variant analysis
Psych HealthPGx Panel RPRD Diagnostics, LLC United States	40	13	D Deletion/duplication analysis T Targeted variant analysis
Whole Pharmacogenomics Scan RPRD Diagnostics, LLC United States	107	69	D Deletion/duplication analysis T Targeted variant analysis
RightMed Mental Health test OneOme, LLC United States	6	15	D Deletion/duplication analysis T Targeted variant analysis
Genomind Pharmacogenetic Report Genomind, Inc. Genomind, Inc United States	14	27	T Targeted variant analysis
PGx-NP (Neuro-Psychiatry) SPMED CO., LTD Step forward Personalized Medicine South Korea	51	26	T Targeted variant analysis
iDNA PGx-CNS iDNA Genomics Greece	30	12	T Targeted variant analysis
Polypharmacy Comprehensive Panel Invitae United States	33	24	D Deletion/duplication analysis T Targeted variant analysis
NeuroIDgenetix AltheaDx/Castle Biosciences United States	2	11	D Deletion/duplication analysis T Targeted variant analysis
Pharmacogenetics Panel: Psychotropics ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	8	14	E Sequence analysis of select exons
RightMed Comprehensive Test with Gene Report OneOme, LLC United States	2	25	D Deletion/duplication analysis T Targeted variant analysis
Neurotransmitter Metabolism Deficiency NGS Panel Fulgent Genetics United States	85	101	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Risperidone response Xcode Life India	1	4	T Targeted variant analysis
HTR2C Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5129	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Serotonin Metabolism Deficiency NGS Panel Fulgent Genetics United States	12	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region

Results: 1 to 16 of 16

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.

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Results: 1 to 16 of 16

Results: 1 to 16 of 16