Clinical and research tests for HBG2 - Genetic Testing Registry (GTR) - NCBI

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Results: 1 to 13 of 13

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
HBG2 Gene Cyanosis, transient neonatal NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
HBG2 Gene Hereditary persistence of fetal hemoglobin NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
Fetal hemoglobin quantitative trait locus 1, 141749, Autosomal dominant (Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome) (HBG2 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
Fetal hemoglobin quantitative trait locus 1, 141749, Autosomal dominant (Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome) (HBG2 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
Cyanosis, transient neonatal, 613977, Autosomal dominant; TNCY (Hemoglobinopathy Toms River) (HBG2 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
HBG2 XmnI polymorphism Genetics Service Unit BRIC-National Institute of Biomedical Genomics India	1	1	T Targeted variant analysis
Multiplex Gap PCR for HPFH and Hb Lepore (Hollandia, Washington- Boston, Baltimore) Hemoglobinopathy Reference Laboratory UCSF Benioff Children's Hospital & Research Center Oakland United States	5	4	D Deletion/duplication analysis
MLPA (Multiplex Ligation-Dependent Probe Amplification) for β-globin gene cluster Hemoglobinopathy Reference Laboratory UCSF Benioff Children's Hospital & Research Center Oakland United States	2	4	D Deletion/duplication analysis
Gamma 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
Haematological diseases panel _v.2.0 CGC Genetics Unilabs Portugal	1	344	C Sequence analysis of the entire coding region
Cyanosis, transient neonatal: Full gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Gamma Globin (HBG1 and HBG2) Sequencing ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	2	2	C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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