diff --git a/docs/about/data-clients.rst b/docs/about/data-clients.rst
index 12710a78..b3444d84 100644
--- a/docs/about/data-clients.rst
+++ b/docs/about/data-clients.rst
@@ -6,22 +6,29 @@ Data clients are academic and commercial resources that use CIViC data (for exam
 - `BioDiscovery NxClinical <https://www.biodiscovery.com/products/NxClinical>`_
 - `Biogazelle <https://www.biogazelle.com/>`_
 - `BioGPS <http://biogps.org/plugin/1238/civic/>`_
+- `BioMuta <https://hivelab.biochemistry.gwu.edu/biomuta>`_
 - `Cambridgene <http://www.cambridgene.com/>`_
+- `Cancer Genome Interpreter <https://www.cancergenomeinterpreter.org/>`_
 - `CancerStop Android Application <https://play.google.com/store/apps/details?id=com.sequilabs.cancerstop>`_
 - `CBioPortal <http://www.cbioportal.org/>`_
+- `C-CAT <https://www.ncc.go.jp/en/c_cat/index.html>`_
 - `CIViC Compass <https://civiccompass.vercel.app/>`_
 - `CIViCmine <http://bionlp.bcgsc.ca/civicmine/>`_
 - `ClinGen Variant Curation Interface (VCI) <https://curation.clinicalgenome.org/>`_
 - `DAPHNI – A platform for precision medicine of multiple myeloma <http://ascopubs.org/doi/10.1200/PO.18.00019>`_
 - `Database of Curated Mutations (DoCM) <http://www.docm.info/>`_
-- `ETH Nexus Personalized Health Technologies - Swiss Variant Interpretation Platform for Oncology <http://www.nexus.ethz.ch/>`_
-- `Euformatics OmnomicsNGS <http://euformatics.com/ongs/>`_
+- `DNAnexus Cohort Browser <https://documentation.dnanexus.com/user/cohort-browser/analyzing-somatic-variants#viewing-gene-and-sample-details>`_
+- `ETH Nexus Personalized Health Technologies - Swiss Variant Interpretation Platform for Oncology <https://www.nexus.ethz.ch/>`_
+- `Euformatics OmnomicsNGS <https://euformatics.com/>`_
 - `Gemini <http://gemini.readthedocs.io/en/latest/>`_
 - `Geneyx Analysis, WES and WGS data analysis & Interpretation platform <https://geneyx.com/geneyxanalysis/>`_
 - `Genome Nexus <https://www.genomenexus.org/>`_
+- `Genomize <https://genomize.com/about_us/>`_
+- `GenomOncology <https://genomoncology.com/about-us/>`_
 - `Genoox <https://www.genoox.com/>`_
 - `GoldenHelix - VSClinical <http://goldenhelix.com/products/VarSeq/vsclinical.html>`_
 - `Hartwig Medical Foundation <https://www.hartwigmedicalfoundation.nl/en/>`_
+- `Illumina Connected Insights <https://assets.illumina.com/products/by-type/informatics-products/connected-insights.html>`_
 - `Johns Hopkins Molecular Tumor Board <https://www.hopkinsmedicine.org/news/articles/the-gaitway-tumor-board>`_
 - `International Cancer Genome Consortium (ICGC) Data Portal <https://dcc.icgc.org/>`_
 - `LifeMap Sciences’ GeneCards Knowledgebase Suite <https://www.genecards.org>`_
@@ -30,18 +37,30 @@ Data clients are academic and commercial resources that use CIViC data (for exam
 - `Microsoft Research - Natural Language Processing <https://www.microsoft.com/en-us/research/wp-content/uploads/2017/05/tacl17.pdf>`_
 - `MolecularMatch <https://www.molecularmatch.com/>`_
 - `Monarch Initiative (via Wikidata) <https://monarchinitiative.org/>`_
-- `My Variant Info <http://myvariant.info/>`_
+- `MyVariant.info <https://myvariant.info/>`_
 - `Monarch Iniative SEPIO - Scientific Evidence and Provenance Information Ontology <https://github.com/monarch-initiative/SEPIO-ontology>`_
-- `NDEx - The Network Data Exchange <http://www.ndexbio.org>`_
+- `NDEx - The Network Data Exchange <https://www.ndexbio.org/>`_
+- `NGeneBio <https://www.ngenebio.com/en/sub/company/about.asp>`_
 - `OncoMX <https://www.oncomx.org/>`_
-- `PathOS - Peter MacCallum Cancer Centre <https://www.petermac.org/about/signature-centres/centre-clinical-cancer-genomics/molecular-diagnostic-software>`_
-- `ProteinPaint <https://pecan.stjude.cloud/proteinpaint>`_
+- `PathOS - Peter MacCallum Cancer Centre <https://github.com/PapenfussLab/PathOS>`_
+- `ProteinPaint <https://proteinpaint.stjude.org/>`_
+- `Rancho BioSciences <https://ranchobiosciences.com/who-we-are>`_
+- `SciLifeLab Molecular Tumor Board Portal <https://www.scilifelab.se/news/portal-to-help-interpret-cancer-data-developed-first-patients-selected/>`_
 - `Smart Cancer Navigator <https://smart-cancer-navigator.github.io/app>`_
 - `SoftGenetics - Geneticist Assistant NGS Interpretative Workbench <https://softgenetics.com/>`_
 - `SolveBio <https://www.solvebio.com/>`_
 - `TCGA Next-Gen Clustered Heat Map Compendium <http://tcga.ngchm.net/>`_
 - `The Hyve <https://thehyve.nl/solutions/cbioportal/>`_
+- `Treehouse Childhood Cancer Initiative <https://treehousegenomics.ucsc.edu/>`_
 - `UCSC Genome Browser (My Data -> Track Hubs -> Cancer Genomics Tracks) <https://genome.ucsc.edu/cgi-bin/hgHubConnect>`_
+- `VA National Precision Oncology Program <https://www.research.va.gov/research_in_action/Precision-Oncology-Program.cfm>`_
 - `Variant Interpretation for Cancer Consortium (VICC) <http://cancervariants.org/>`_
 - `VarSome <https://varsome.com/>`_
+- `Velsera <https://velsera.com/about-us/>`_
 - `Wikidata <https://www.wikidata.org/>`_
+
+Data Distribution
+-----------------
+CIViC data are also available through:
+
+- `CIViC on the AWS Registry of Open Data <https://registry.opendata.aws/civic/>`_