Clinical and research tests for C0027819 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States	97	77	C Sequence analysis of the entire coding region
CNS Tumor Classification by Methylation Array Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States	9	2	M Methylation analysis
NGS Neuroblastoma Panel Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States	1	8	C Sequence analysis of the entire coding region
Cancer Hotspot Panel Genome-Nilou Lab Iran	45	34	E Sequence analysis of select exons
MYCN (N-Myc) Amplification Detection for Neuroblastoma Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States	1	1	I FISH-interphase
Targeted Oncology Microarray Analysis Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States	7	7	D Deletion/duplication analysis
Neuroblastoma, 256700, Autosomal dominant, Isolated cases (Neuroblastoma) (NME1 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
Neuroblastoma, susceptibility to, 1, 256700, Autosomal dominant, Isolated cases (Neuroblastoma) (KIF1B 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
Pediatric Cancer Panel PreventionGenetics, part of Exact Sciences United States	78	64	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
PrimBio Cancer HotSpot Panel PrimBio Research Institute United States	60	50	T Targeted variant analysis
Neuroblastoma Panel PreventionGenetics, part of Exact Sciences United States	3	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cancer Panel PreventionGenetics, part of Exact Sciences United States	122	117	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
MitoMet®Plus aCGH Analysis Baylor Genetics United States	842	637	D Deletion/duplication analysis
Hereditary Neuroblastoma via the KIF1B Gene PreventionGenetics, part of Exact Sciences United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Neuroblastoma Liquid Biopsy Panel (Circulating Tumor DNA) Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	1	23	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Neuroblastoma (sequence analysis of NME1 gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States	416	235	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neuroblastoma , Panel Massive Sequencing (NGS) 4 Genes Reference Laboratory Genetics Spain	3	4	C Sequence analysis of the entire coding region
FISH - Solid Tumor Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab) United States	22	41	F Fluorescence in situ hybridization (FISH)
Central Hypoventilation and Apnea Panel Blueprint Genetics Finland	4	15	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.