{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["LESTR","NPY3R","HM89","NPYY3R","D2S201E","fusin","HSY3RR","NPYR","CD184"],"biotype":"protein_coding","hgnc_id":"HGNC:2561","gene_name":"C-X-C motif chemokine receptor 4","omim_gene":["162643"],"alias_name":null,"gene_symbol":"CXCR4","hgnc_symbol":"CXCR4","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"2:136871919-136875735","ensembl_id":"ENSG00000121966"}},"GRch38":{"90":{"location":"2:136114349-136118165","ensembl_id":"ENSG00000121966"}}},"hgnc_date_symbol_changed":"1998-09-17"},"entity_type":"gene","entity_name":"CXCR4","confidence_level":"3","penetrance":null,"mode_of_pathogenicity":"Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","publications":["12692554","15536153"],"evidence":["NHS GMS","North West GLH","London North GLH","IUIS Classification February 2018","Victorian Clinical Genetics Services","Expert 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