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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Invitae Expanded Renal Disease Panel Invitae United States | 693 | 388 |
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SIX1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 498 | 498 |
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Centogene AG - the Rare Disease Company Germany | 499 | 499 |
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Centogene AG - the Rare Disease Company Germany | 203 | 194 |
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Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel Invitae United States | 67 | 41 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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Invitae Progressive Renal Disease Panel Invitae United States | 310 | 195 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
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Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Panel PreventionGenetics, part of Exact Sciences United States | 82 | 77 |
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Branchiootorenal Syndrome Panel PreventionGenetics, part of Exact Sciences United States | 3 | 3 |
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Branchiootorenal Syndrome via the SIX1 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
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Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
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Nonsyndromic Hearing Loss NGS Panel Fulgent Genetics United States | 146 | 99 |
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Fulgent Genetics United States | 43 | 15 |
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Fulgent Genetics United States | 68 | 41 |
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Branchiootorenal Spectrum Disorders NGS Panel Fulgent Genetics United States | 6 | 3 |
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Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics Inc United States | 249 | 184 |
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BOR SYNDROME (BRANCHIO-OTO-RENAL) Laboratorio de Genetica Clinica SL Spain | 3 | 3 |
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