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
ALX4	gene	ALX4	Expert Review Green;NHS GMS	Test panel testing 2020-07-27			BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Parietal foramina 2, (AD), 609597;Frontonasal dysplasia 2, (AR), 613451;Parietal foramina				29215649;22829454;29681084		False	3	0;100;0	1.15	False		ENSG00000052850	ENSG00000052850	HGNC:450													
ISCA-37390-Loss	region		Expert Review Green;Expert Review	Test panel testing 2020-07-27			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown							False	3	100;0;0	1.15	False					5			37695	11347150				3		80	small	5p15 terminal (Cri du chat syndrome) region Loss