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Ambry Genetics' multi-gene blood tests for inherited cancer risk: CancerNext covers 41 genes and CancerNext-Expanded 90, ordered through a clinician.
Registered in the NIH Genetic Testing Registry by Ambry Genetics (CLIA 05D0981414): CancerNext, GTR000560509.15 (41 genes, version updated 19 May 2026), and CancerNext-Expanded, GTR000560508.11 (90 genes, updated 14 February 2025), which adds genes for haematological predisposition (DDX41, RUNX1, GATA2, CEBPA, ETV6), pancreatitis (PRSS1, SPINK1, CTRC, CPA1), paraganglioma, rhabdoid tumour and others. Versions with paired RNA analysis (RNAinsight) are registered separately. GTR records them as tests developed by the laboratory; they are not among the FDA-authorised hereditary cancer products.
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Query for this drug: (TITLE:"CancerNext and CancerNext-Expanded" OR ABSTRACT:"CancerNext and CancerNext-Expanded" OR TITLE:"Ambry Genetics" OR ABSTRACT:"Ambry Genetics" OR TITLE:"CancerNext" OR ABSTRACT:"CancerNext" OR TITLE:"CancerNext-Expanded" OR ABSTRACT:"CancerNext-Expanded" OR TITLE:"Ambry CancerNext" OR ABSTRACT:"Ambry CancerNext") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about CancerNext and CancerNext-Expanded (Ambry Genetics), not a curated reading list.
Shares Peutz-Jeghers syndrome, MSH2, MLH1, PALB2 and the tags test, hereditary.
Shares MSH2, MLH1, Lynch syndrome, Hereditary cancer syndromes and the tags test, hereditary.
Shares MSH2, MLH1, PALB2, Lynch syndrome and the tags test, hereditary.
Shares MSH2, MLH1, PALB2, Lynch syndrome and the tags test, hereditary.
Shares MSH2, MLH1, PALB2, Lynch syndrome and the tags test, hereditary.
Shares Peutz-Jeghers syndrome, MSH2, MLH1, PALB2 and the tags test, hereditary.
Shares GATA2, RUNX1, PALB2, Hereditary cancer syndromes and the tags test, hereditary.
Shares Ambry Genetics, PALB2, Hereditary cancer syndromes, BRCA1 / BRCA2 (HRD) and the tags test, hereditary.
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