MTHFR - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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CentoNeuro Panel Centogene AG - the Rare Disease Company Germany | 1886 | 1858 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Intellectual Disability Panel Centogene AG - the Rare Disease Company Germany | 777 | 770 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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CentoMito Comprehensive Panel Centogene AG - the Rare Disease Company Germany | 406 | 414 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences United States | 346 | 160 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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Invitae Comprehensive Neurometabolic Disorders Panel Invitae United States | 351 | 249 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States | 297 | 180 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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Invitae Neonatal Respiratory Distress Panel Invitae United States | 163 | 111 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (CHI3L1 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (HTR2A 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
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Schizophrenia, 181500, Autosomal dominant (DAO 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (SYN2 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (COMT 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (RTN4R 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (DRD3 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
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Schizoaffective disorder, susceptibility to, 181500, Autosomal dominant (DISC1 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
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Schizophrenia, 181500, Autosomal dominant (APOL2 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (MTHFR 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
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Schizophrenia, 181500, Autosomal dominant (DAOA 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
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Schizophrenia, susceptibility to, 181500, Autosomal dominant (AKT1 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
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