Accelerate NGS variant interpretation with rapid search and insight into the full text of the genomic literature
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Explore our platforms for germline and somatic variant interpretation
Access article information on more than 26 million variants, as well as curated germline variant content.
Our Cancer Knowledgebase is used to interpret cancer variants, connecting them to therapies and clinical trials
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Gain access to an expansive, constantly updated database of curated genomic information
