The Database of Genomic Variants is a curated catalog of human structural variation, with browser, download, query, and submission tools.
DISGENET
vsPSnpBind
DISGENET vs PSnpBind
How do DISGENET and PSnpBind compare? Here are the facts side by side: pricing, platforms, open-source status and what each one is for.
| Directory detail | DISGENET | PSnpBind |
|---|---|---|
| What it is | DISGENET provides curated gene-disease and variant-disease associations, with a REST API, R package, and Cytoscape app. | PSnpBind catalogs protein variants and their effects on protein-ligand binding affinity. |
| Website | ||
| Type | Website | Website |
| Topic | ||
| Pricing | Not confirmed | Not confirmed |
| Platforms | Web | Web |
| Open source | Not stated | Not stated |
| Language | English | English |
| Alternatives |
Other options to consider
Sites similar to both DISGENET and PSnpBind.
LOVD is an open-source system for displaying gene-centered DNA variants and finding locus-specific databases.
HGVD provides a searchable catalog of genetic variants and allele frequencies focused on the Japanese population.
Search structural variants in autism spectrum disorder through the Autism Chromosome Rearrangement Database.
Stanford’s Coronavirus Antiviral and Resistance Database records published data on SARS-CoV-2 variant susceptibility and spike mutations.
The Monarch Initiative integrates and aligns cross-species data on genes, genotypes, variants, diseases, and phenotypes.