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MCG CNV Database

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About Human genome variation database

This human genome variation database is a repository system and has been constructed to achieve permanent data management and information sharing of human mutation data. The human genome variation database contains various variation data not only mutations and short/long insertions/deletions, but also structural variations and repeat variations with statistical genetics analysis results and provides cross-search between disease and variations to overview disease mechanisms. Currently this database contains information extracted from scientific papers and next generation sequencing results and other small scale experimental results of several research laboratories. We greatly appreciate your mutation data submission.
This work has been supported by the Japan science and Technology Agency.

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Browse by chromosome

Overview of SNP density

Summary of all diseases


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Search by gene name

keyword
include search:
GWAS-DB SNP-DB CNV-DB CNV association DB HLA-DB

Search by disease name

keyword
include search:
GWAS-DB CNV association DB HLA-DB

Search by genomic position

ChrNo. Region -
include search:
GWAS-DB SNP-DB CNV-DB CNV association DB HLA-DB

Search by SNP number

kind keyword
include search:
GWAS-DB SNP-DB CNV-DB CNV association DB HLA-DB

Interaction view by gene name

keyword