Tempus xT Tempus AI - RTP United States | 2 | 647 | - I Microsatellite instability testing (MSI)
- C Sequence analysis of the entire coding region
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IFNGR1 Gene Mycobacterial infection, atypical, familial disseminated NGS Genetic DNA Test DNA Labs India India | 1 | 1 | - S Mutation scanning of the entire coding region
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IFNGR1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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CentoImmuno Panel Centogene AG - the Rare Disease Company Germany | 323 | 329 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Invitae Inborn Errors of Immunity and Cytopenias Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 754 | 562 | - D Deletion/duplication analysis
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MayoComplete Solid Tumor Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 476 | - I Microsatellite instability testing (MSI)
- R RNA analysis
- C Sequence analysis of the entire coding region
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JAX SOMASEQ The Jackson Laboratory for Genomic Medicine United States | 1 | 517 | - D Deletion/duplication analysis
- I Microsatellite instability testing (MSI)
- R RNA analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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Endeavor PathGroup United States | 73 | 505 | - C Sequence analysis of the entire coding region
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OmniSeq INSIGHT OmniSeq, Inc. United States | 1 | 525 | - R RNA analysis
- C Sequence analysis of the entire coding region
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Mendelian Susceptibility to Mycobacterial Disease Panel PreventionGenetics, part of Exact Sciences United States | 29 | 17 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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H. pylori infection, susceptibility to, 600263 (IFNGR1 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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Hepatitis B virus infection, susceptibility to, 610424 (IFNGR1 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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Immunodeficiency 27A, mycobacteriosis, AR, 209950, Autosomal recessive; IMD27A (Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency) (IFNGR1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Immunodeficiency 27B, mycobacteriosis, AD, 615978, Autosomal dominant; IMD27B (Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency) (IFNGR1 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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Immunodeficiency 27A, mycobacteriosis, AR, 209950, Autosomal recessive; IMD27A (Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency) (IFNGR1 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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Immunodeficiency 27B, mycobacteriosis, AD, 615978, Autosomal dominant; IMD27B (Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency) (IFNGR1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Tuberculosis, susceptibility to, 607948 (Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency) (IFNGR1 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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Tuberculosis infection, protection against, 607948 (Tuberculosis) (IFNGR1 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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ProvSeq 523 Providence St. Joseph Health Molecular Genomics Laboratory Providence St Joseph Health United States | 1 | 523 | - C Sequence analysis of the entire coding region
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Invitae Primary Immunodeficiency Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 552 | 424 | - D Deletion/duplication analysis
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