How to find the position of genes that their variants called by hs37d5?

Question

[Zahra]

Hi all,

I have used the PCAWG vcf files for my analysis. These variants have been called by the hs37d5 reference genome. Now I want to subset the list of my interest gene from these vcf files and don't know how to find the start and end positions.

Thanks for any help.

[Pierre Lindenbaum]

The genome build is GRCH37: https://www.gencodegenes.org/human/release_19.html