NewbornGeneID GeneID Lab - Advanced Molecular Diagnostics
United States | 73 | 61 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
MYH11 - NGS including CNV analysis Centogene AG - the Rare Disease Company
Germany | 3 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Invitae Connective Tissue Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp
United States | 195 | 92 | - D Deletion/duplication analysis
|
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
|
Marfan Syndrome and Related Aortopathies Panel PreventionGenetics, part of Exact Sciences
United States | 40 | 38 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders NGS panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
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
|
Aortic aneurysm, familial thoracic 4, 132900, Autosomal dominant; AAT4 (Familial thoracic aortic aneurysm and aortic dissection) (MYH11 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
|
Invitae Genetic Health Screen Labcorp Genetics (formerly Invitae) LabCorp
United States | 409 | 164 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Invitae Cardio Screen Labcorp Genetics (formerly Invitae) LabCorp
United States | 208 | 81 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Invitae 78 Gene Actionable Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp
United States | 220 | 75 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Connective Tissue Disorders Panel PreventionGenetics, part of Exact Sciences
United States | 166 | 101 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
TAADNext® Ambry Genetics
United States | 50 | 35 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
FBN1 gene sequence and deletion/duplication reflex to TAADNext® Ambry Genetics
United States | 50 | 35 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
CustomNext-Cardio® Ambry Genetics
United States | 236 | 167 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders NGS panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
