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Annotation for non-coding pathogenic variants in humans

Hello all,

I am exploring ClinVar database from NCBI that catalogues clinical variants for humans. As I understand, most of these variants are annotated in coding regions (or at least I was unable to find variants for the whole genome irrespective of whether coding or non-coding). I was wondering if anyone knew of such a database where I could also find an equivalent annotation of noncoding variants.

Thanks for any help! :) Manas

interpretation pathogenic variant clinvar

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