Clinical and research tests for C4552766 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
G-Banded Chromosome Analysis Cytogenetics Laboratory University Of Washington United States	16	6	K Karyotyping
کاریوتایپ خون Razi Pathobiology & Medical Genetics laboratory Iran	8	6	K Karyotyping
IFISH for Aneuploidy (Products of Conception) Cytogenetics Laboratory University Of Washington United States	12	7	I FISH-interphase
Standard karyotype (pediatric) Allele Diagnostics United States	16	6	K Karyotyping
IriSight™ for Pregnancy Loss Variantyx, Inc. United States	3	2	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Anora Products of Conception Testing Natera, Inc. United States	4	1	K Karyotyping D Deletion/duplication analysis H Detection of homozygosity U Uniparental disomy study (UPD)
Constitutional Chromosomal Microarray Analysis Clinical Genomics Laboratory Laboratory for Precision Diagnostics, University of Washington United States	26	1	D Deletion/duplication analysis
Chromosome Analysis, Congenital, Blood Mayo Clinic Laboratories Mayo Clinic United States	11	1	K Karyotyping
Cytogenomic Molecular Inversion Probe Array FFPE Tissue - Products of Conception ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories United States	15	1	K Karyotyping
Chromosome Analysis with Reflex to Genomic Microarray ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories United States	16	1	K Karyotyping D Deletion/duplication analysis H Detection of homozygosity
Chromosome Analysis, Tissue w/ Reflex to Microarray, ClariSure(R) Oligo-SNP Quest Diagnostics Nichols Institute San Juan Capistrano United States	2	1	K Karyotyping D Deletion/duplication analysis
Thrombosis Disorder NGS Panel Fulgent Genetics United States	46	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States	1048	472	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Thrombosis, Platelet Disorder, and Coagulation Deficiency NGS Panel Fulgent Genetics United States	146	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Afibrinogenemia NGS Panel Fulgent Genetics United States	13	3	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FGG Single Gene Fulgent Genetics United States	11	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
FGB Single Gene Fulgent Genetics United States	12	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Chromosome Analysis: Karyotype Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States	20	1	K Karyotyping
Coagulation Deficiency NGS Panel Fulgent Genetics United States	56	24	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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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.