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How does dbVar place data submitted on one assembly (e.g., NCBI36) on other assemblies (e.g., GRCh37)?

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dbVar uses NCBI’s Remap tool to map variants between assemblies. All variants reported in human-based studies are automatically remapped to both NCBI36 and GRCh37. More information on use the tool and a list of supported assemblies can be found on the Remap website.

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