Clinical and research tests for ZIC3 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 96

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hydrocephalus Panel PreventionGenetics, part of Exact Sciences United States	41	38	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Congenital heart disease Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	1	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital heart disease Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Congenital heart disease NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	15	C Sequence analysis of the entire coding region T Targeted variant analysis
Nonsyndromic Congenital Heart Disease Panel PreventionGenetics, part of Exact Sciences United States	54	44	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Heterotaxy, visceral, 1, X-linked, 306955, X-linked recessive; HTX1 (Heterotaxia) (ZIC3 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
Heterotaxy, visceral, 1, X-linked, 306955, X-linked recessive; HTX1 (Heterotaxia) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
Heterotaxy, visceral, 1, X-linked, 306955, X-linked recessive; HTX1 (Heterotaxia) (ZIC3 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
Heterotaxy, visceral, 1, X-linked, 306955, X-linked recessive; HTX1 (Heterotaxia) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
VACTERL association, X-linked, 314390, X-linked recessive; VACTERLX (VACTERL with hydrocephalus) (ZIC3 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
VACTERL association, X-linked, 314390, X-linked recessive; VACTERLX (VACTERL with hydrocephalus) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
VACTERL association, X-linked, 314390, X-linked recessive; VACTERLX (VACTERL with hydrocephalus) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
VACTERL association, X-linked, 314390, X-linked recessive; VACTERLX (VACTERL with hydrocephalus) (ZIC3 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
Congenital heart defects, nonsyndromic, 1, X-linked, 306955, X-linked recessive (Heterotaxia) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
Congenital heart defects, nonsyndromic, 1, X-linked, 306955, X-linked recessive (Heterotaxia) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	D Deletion/duplication analysis
Congenital heart defects, nonsyndromic, 1, X-linked, 306955, X-linked recessive (Heterotaxia) (ZIC3 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
Congenital heart defects, nonsyndromic, 1, X-linked, 306955, X-linked recessive (Heterotaxia) (ZIC3 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
qChip 180 Quantitative Genomic Medicine Laboratories, SL Spain	184	162	D Deletion/duplication analysis
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States	223	201	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hydrocephalus Panel Genetic Services Laboratory University of Chicago United States	3	16	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 96

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.