Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
ATP7B	gene	ATP7B	Expert Review Green;NHS GMS	Wilson disease		Gastrohepatology	BIALLELIC, autosomal or pseudoautosomal	Wilson disease, OMIM:277900;Wilson disease, MONDO:0010200						False	3	100;0;0	1.3	False		ENSG00000123191	ENSG00000123191	HGNC:870