Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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CGC Genetics Unilabs Portugal | 1 | 33 |
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CGC Genetics Unilabs Portugal | 1 | 385 |
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CGC Genetics Unilabs Portugal | 1 | 2 |
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Hereditary angioedema type 1 (sequence analysis of SERPING1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Immunodeficiencies and Immunologic Diseases Panel (Complete) Mendelics Brazil | 1 | 397 |
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Plugin system clutter panel. NGS panel of 75 genes. Genologica Medica Spain | 76 | 75 |
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Complement component 4, partial deficiency of: Full gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
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Angioedema, hereditary: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 4 | 4 |
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Angioedema, hereditary, types I and II Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 1 |
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Angioedema, hereditary, types I and II Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany | 1 | 1 |
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Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center Turkey | 1 | 1 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
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Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
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GeneDx United States | 1 | 1040 |
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Two Known Familial Variants in a Nuclear Gene GeneDx United States | 1 | 1043 |
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One Known Familial Variant in a Nuclear Gene GeneDx United States | 1 | 1045 |
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Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 28 | 33 |
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NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
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Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
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