Database

VarySysDB

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NameVarySysDB
AliasesNone
DescriptionThis is a system to search, display, and download our research results on human polymorphism based on publicly available data and annotations of transcripts presented by H-InvDB. It provides information about single nucleotide polymorphisms (SNPs), deletion-insertion polymorphisms (DIPs), short tandem repeats (STRs), single amino acid repeats (SARs), structural variation (or copy number variations: CNVs), and their relations to the genome, transcripts, and functional domains.
TypeDB
Main Institutes of managementMolecular Profiling Research Center for Drug Discovery (molprof), National Institute of Advanced Industrial Science and Technology (AIST)
Country of the InstituteJapan
URL of the sitehttp://h-invitational.jp/varygene/home.htm
InterfaceSearch site
Input examplePut down "HIX" etc. in the input form on upper right of top page and click "GO" button.
KeywordTranscriptional product
Amount of the all data for download(Mbyte) | Method to obtain the all data.-|None
External resources (databases) in building the product.H-InvDB | dbSNP
Data type
Biological species in the main concernHomo sapiens [Taxonomy_id: 9606, human]
Conditions of useCC BY-SA 2.1 JP
Frequency of updates (in last two years)1
Last date of updates (date of confirmation)2015/04/02 (2019/07/04)
Main IDs used in the productsH-Inv cluster ID (HIX) | HUGO gene symbol
How to make a link to get access to each IDs.None
external databases to which this database/tool have linksNone
Published papers (PubMed IDs)None
Operational Statusavailable