Clinical and research tests for C1836706 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Solid Tumor Panel Centogene AG - the Rare Disease Company Germany	218	135	C Sequence analysis of the entire coding region
TSHR - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany	3	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hyperthyroidism, nonautoimmune, 609152, Autosomal dominant, Isolated cases (Familial hyperthyroidism due to mutations in TSH receptor) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
Hyperthyroidism, nonautoimmune, 609152, Autosomal dominant, Isolated cases (Familial hyperthyroidism due to mutations in TSH receptor) (TSHR 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
Invitae Comprehensive Carrier Screen Invitae United States	886	547	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Hypothyroidism and Thyroid Hormone Resistance Panel PreventionGenetics, part of Exact Sciences United States	32	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hypothyroidism [Congenital, Nongoitrous] and Hyperthyroidism [Familial Gestational and Nonautoimmune] via the TSHR Gene PreventionGenetics, part of Exact Sciences United States	3	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Congenital Hypothyroidism Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	18	15	C Sequence analysis of the entire coding region
Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes. Genologica Medica Spain	42	21	C Sequence analysis of the entire coding region
Hypothyroidism and Resistance to Thyroid Hormone NGS Panel Fulgent Genetics United States	41	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Familial Thyroid Dyshormogenesis , Panel Massive Sequencing (NGS) 10 Genes Reference Laboratory Genetics Spain	14	10	C Sequence analysis of the entire coding region
Hypothyroidism and Thyroid Hormone Resistance Asper Biogene Asper Biogene LLC Estonia	29	22	C Sequence analysis of the entire coding region
Familial Non-Autoimmune Hyperthyroidism , Sequencing TSHR Gene Reference Laboratory Genetics Spain	1	1	C Sequence analysis of the entire coding region
Comprehensive Hereditary Cancer Panel Baylor Genetics United States	132	61	E Sequence analysis of select exons
Hereditary Endocrine Cancer Panel Baylor Genetics United States	51	15	E Sequence analysis of select exons
TSHR Gene Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States	3	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Familial non-immune hyperthyroidism Bioarray Spain	1	1	C Sequence analysis of the entire coding region
Single gene testing TSHR CeGaT GmbH Germany	3	1	C Sequence analysis of the entire coding region
TSHR Single Gene Fulgent Genetics United States	3	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

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