Clinical and research tests for C0020598 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 16 of 16

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Abnormal mineralization disorders Deletion/ Duplication Panel HNL Genomics Connective Tissue Gene Tests United States	2	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Abnormal mineralization disorders Comprehensive Panel HNL Genomics Connective Tissue Gene Tests United States	2	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Abnormal mineralization disorders Deletion/ Duplication Panel HNL Genomics Connective Tissue Gene Tests United States	2	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Abnormal mineralization disorders Comprehensive Panel HNL Genomics Connective Tissue Gene Tests United States	2	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Abnormal mineralization disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States	2	15	C Sequence analysis of the entire coding region T Targeted variant analysis
Hypomagnesemia NGS Panel Fulgent Genetics United States	121	23	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States	1048	473	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neuronal Migration Disorders NGS Panel Fulgent Genetics United States	392	83	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Abnormal mineralization disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States	2	15	C Sequence analysis of the entire coding region T Targeted variant analysis
Hypoparathyroidism panel Genetic Services Laboratory University of Chicago United States	21	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region
HIRA Single Gene Fulgent Genetics United States	85	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
ARVCF Single Gene Fulgent Genetics United States	85	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FAT4 Single Gene Fulgent Genetics United States	91	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FAM111A Single Gene Fulgent Genetics United States	90	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Full Comprehensive Cancer Panel Fulgent Genetics United States	1166	141	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5130	4674	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.