Filters
reset allTests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Neurofibromatosis, type 2, 101000, Autosomal dominant; NF2 (Neurofibromatosis type 2) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Invitae United States | 409 | 164 |
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Invitae United States | 160 | 62 |
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Invitae 78 Gene Actionable Disorders Panel Invitae United States | 220 | 75 |
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Variant Resolution Test for CustomNext-Cancer® (+RNAinsight®) Ambry Genetics United States | 147 | 18 |
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Variant Resolution Test for BrainTumorNext® (+RNAinsight®) Ambry Genetics United States | 72 | 8 |
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Variant Resolution Test for CancerNext-Expanded® (+RNAinsight®) Ambry Genetics United States | 95 | 71 |
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PreventionGenetics, part of Exact Sciences United States | 78 | 64 |
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NF2 gene sequence and deletion/duplication Ambry Genetics United States | 3 | 1 |
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Ambry Genetics United States | 147 | 91 |
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Ambry Genetics United States | 122 | 71 |
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Ambry Genetics United States | 72 | 29 |
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Neurofibromatosis and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 6 |
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Neurofibromatosis and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 6 |
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Neurofibromatosis and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 6 |
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Noonan spectrum disorder Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 25 |
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Noonan spectrum disorder Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 25 |
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Meningiomatosis/ Multiple Meningioma NGS Panel Medical Genomics Laboratory Department of Genetics UAB United States | 4 | 4 |
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