CLINICAL
Gene Variant Databases
Uncover critical and timely genomics insights with QIAGEN’s trusted portfolio of hereditary and somatic gene variant databases powered by augmented molecular intelligence.
Germline and Somatic Databases
Human Gene Mutation Database (HGMD)
Shorten the diagnostic odyssey with the de-facto standard resource
for identifying inherited disease-causing mutations
Human Somatic Mutation Database (HSMD)
Gain deep insight into clinically observed somatic variants to better understand and define precise function and actionability
Catalogue of Somatic Mutations in Cancer (COSMIC)
Explore the impact of somatic mutations in human cancer with
the world’s largest and most comprehensive resource
QIAGEN Knowlege Base (for Clinical NGS Testing)
The content core of QIAGEN's clinical NGS informatics portfolio with 40+ databases and two decades of expert curation
Live, Interactive Demo - September 15
Get an in-depth look at HSMD
Is your lab currently performing somatic NGS testing, but having difficulty managing increasing numbers of variants of unknown significance and secondary findings? Do you need a faster way to find off-label therapies?
On September 15, join us for a live, interactive demo where our experts will show you how HSMD serves as a single trusted resource for multiple precision oncology and clinical research applications.