LRB-HGVD

HUMAN GENOME VARIATION DATABASE

Human Genome Variation Database (HGVD) provides comprehensive information about Variations found in the Human Genome. HGVD focuses on the relationship between human genome variations and phenotypes. Information in the database is manually curated, verified and updated periodically.

HGVD can be integrated to genome analytical tools to annotate & rank variants based on phenotype and clinical significance. At present HGVD is integrated with Leucine Rich Bio’s Human Genome Variant Analysis platform, AGIS.

HGVD is developed and maintained by Leucine Rich Bio.

Key Features

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COMPREHENSIVE HUMAN GENOME VARIATION INFORMATION.

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VARIANT - CLINICAL SIGNIFICANCE ASSOCIATION.

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VARIANT - PHENOTYPE ASSOCIATION.

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VARIANT - PHARMACOGENOMICS ASSOCIATION.

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