Clinical and research tests for 182135 - Genetic Testing Registry (GTR) - NCBI

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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
GeneSight Psychotropic Assurex Health, Inc. United States	6	14	D Deletion/duplication analysis T Targeted variant analysis
Tempus nP Tempus Labs, Inc. United States	4	13	T Targeted variant analysis
Psychotropic Pharmacogenomics Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	1	22	T Targeted variant analysis
PGx-NP (Neuro-Psychiatry) SPMED CO., LTD Step forward Personalized Medicine South Korea	51	26	T Targeted variant analysis
Anorexia nervosa, susceptibility to, 606788 (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Major depressive disorder, response to citalopram therapy in, 608516 (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Schizophrenia, susceptibility to, 181500, Autosomal dominant (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Seasonal affective disorder, susceptibility to, 608516 (HTR2A gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Seasonal affective disorder, susceptibility to, 608516 (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Obsessive-compulsive disorder, susceptibility to, 164230, Autosomal dominant; OCD (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Alcohol dependence, susceptibility to, 103780, Multifactorial (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
NeuroIDgenetix AltheaDx/Castle Biosciences United States	2	11	D Deletion/duplication analysis T Targeted variant analysis
qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain	3	1969	S Mutation scanning of the entire coding region C Sequence analysis of the entire coding region
Pharmacogenetics Panel: Psychotropics ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	8	14	E Sequence analysis of select exons
Autism Spectrum Gene Panel Duzen Laboratories Duzen BBAGUAS Turkey	1	160	C Sequence analysis of the entire coding region

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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.