Clinical and research tests for C1853761 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 49

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
SETX - Gene sequencing Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands	2	1	C Sequence analysis of the entire coding region
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	3	3	C Sequence analysis of the entire coding region
Neuro-Ophthalmic Disorders NGS Panel Fulgent Genetics United States	52	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Early-Onset Ataxia NGS Panel Fulgent Genetics United States	505	132	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Late-Onset Ataxia NGS Panel Fulgent Genetics United States	133	56	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Ataxia NGS Panel Fulgent Genetics United States	533	149	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Ataxia with Oculomotor Apraxia Type 1/2 NGS Panel Fulgent Genetics United States	3	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
ATAXIA-OCULOMOTOR APRAXIA TYPE 2 (AOA2) Laboratorio de Genetica Clinica SL Spain	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Nonprevalent Amyotrophic Lateral Sclerosis Advanced Sequencing Evaluation Athena Diagnostics United States	24	15	C Sequence analysis of the entire coding region
Ataxia, Comprehensive Evaluation Athena Diagnostics United States	44	42	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Ataxia, Complete Recessive Evaluation Athena Diagnostics United States	21	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Ataxia, Supplemental Recessive Evaluation Athena Diagnostics United States	20	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Oculomotor Apraxia Ataxia Advanced Sequencing Evaluation Athena Diagnostics United States	3	2	C Sequence analysis of the entire coding region
Ataxia, autosomal recessive and X-linked Panel CeGaT GmbH Germany	7	46	C Sequence analysis of the entire coding region
Spinocerebellar ataxia with axonal neuropathy type 2 Bioarray Spain	1	1	C Sequence analysis of the entire coding region
Single gene testing SETX CeGaT GmbH Germany	2	1	C Sequence analysis of the entire coding region
Leukodystrophy / Leukencephalopathy and differential diagnoses Panel CeGaT GmbH Germany	69	175	C Sequence analysis of the entire coding region
Ataxia and differential diagnoses Panel CeGaT GmbH Germany	173	204	C Sequence analysis of the entire coding region
Amyotrophic Lateral Sclerosis (ALS) Panel CeGaT GmbH Germany	29	54	C Sequence analysis of the entire coding region
Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel CeGaT GmbH Germany	147	143	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 49

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: 21 to 40 of 49

Results: 21 to 40 of 49