Clinical and research tests for C3161174 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 53

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
MLPA (Multiplex Ligation-Dependent Probe Amplification) for α-Globin cluster Hemoglobinopathy Reference Laboratory UCSF Benioff Children's Hospital & Research Center Oakland United States	5	3	D Deletion/duplication analysis
Alpha thalassemia, the most common deletions (Alpha Multiplex GAP-PCR) Hemoglobinopathy Reference Laboratory UCSF Benioff Children's Hospital & Research Center Oakland United States	3	2	D Deletion/duplication analysis
Alpha globin gene sequencing Hemoglobinopathy Reference Laboratory UCSF Benioff Children's Hospital & Research Center Oakland United States	4	2	C Sequence analysis of the entire coding region
Alpha Thalassemia Deletion/Duplication and Constant Spring Panel PreventionGenetics, part of Exact Sciences United States	2	2	D Deletion/duplication analysis
Alpha Thalassemia Panel PreventionGenetics, part of Exact Sciences United States	2	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Alpha Globin Gene Sequencing UCSF Molecular Diagnostics Laboratory University of California, San Francisco United States	4	2	C Sequence analysis of the entire coding region
Alpha Thalassemia Deletions UCSF Molecular Diagnostics Laboratory University of California, San Francisco United States	3	2	D Deletion/duplication analysis
M Beacon Focus B; 14 Genes Fulgent Genetics United States	17	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Alpha thalassemia Molecular Genetics Laboratory BC Children's and BC Women's Hospitals Canada	8	2	T Targeted variant analysis
Alpha Thalassemia (HBA1 and HBA2) Deletion/Duplication with reflex to Hb Constant Spring, Fetal ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	3	2	D Deletion/duplication analysis E Sequence analysis of select exons
Alpha Thalassemia (HBA1 and HBA2) Deletion/Duplication with reflex to Hb Constant Spring ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	3	2	D Deletion/duplication analysis E Sequence analysis of select exons
Beacon Ashkenazi Jewish Male Carrier Screening Panel Fulgent Genetics United States	145	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Erythrocytosis NGS Panel Fulgent Genetics United States	61	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Ashkenazi Jewish Female Carrier Screening Panel Fulgent Genetics United States	148	42	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States	718	337	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon ACOG/ACMG Female Carrier Screening Panel Fulgent Genetics United States	16	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Expanded Male Carrier Screening Panel Fulgent Genetics United States	638	300	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon ACOG/ACMG Male Carrier Screening Panel Fulgent Genetics United States	13	5	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States	663	308	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Beacon Ashkenazi Jewish Male Carrier Screening Panel Fulgent Genetics United States	145	41	D Deletion/duplication analysis 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.