Clinical and research tests for C0266313 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Invitae Renal Tubular Disorders Panel Invitae United States	68	39	D Deletion/duplication analysis
Invitae Neonatal Respiratory Distress Panel Invitae United States	163	111	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Inherited Kidney Diseases Panel PreventionGenetics United States	10	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Renal tubular dysgenesis, 267430, Autosomal recessive; RTD (Renal tubular dysgenesis) (REN gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
Preeclampsia, susceptibility to (AGT gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
Renal tubular dysgenesis, 267430, Autosomal recessive (Renal tubular dysgenesis) (AGTR1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
Renal tubular dysgenesis, 267430, Autosomal recessive (Renal tubular dysgenesis) (AGT gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
Renal tubular dysgenesis, 267430, Autosomal recessive (Renal tubular dysgenesis) (ACE gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
SARS, progression of (ACE gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
Myocardial infarction, susceptibility to (ACE gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
[Hyperproreninemia] (Renal tubular dysgenesis) (REN gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
[Angiotensin I-converting enzyme, benign serum increase] (ACE gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre Turkey	1	1	C Sequence analysis of the entire coding region
RenalZoom Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States	527	338	C Sequence analysis of the entire coding region
Renal tubular dysgenesis NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	4	C Sequence analysis of the entire coding region T Targeted variant analysis
Renal tubular dysgenesis Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	4	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Renal tubular dysgenesis Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	1	4	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Panel PreventionGenetics United States	40	53	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Autosomal Recessive Renal Tubular Dysgenesis (RTD) via the ACE Gene PreventionGenetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Autosomal Recessive Renal Tubular Dysgenesis (RTD) Panel PreventionGenetics United States	1	4	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Autosomal Recessive Renal Tubular Dysgenesis (RTD) via the REN Gene PreventionGenetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis

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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.