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
ASCL1	gene	ASCL1	Expert Review Amber;Victorian Clinical Genetics Services	Central Hypoventilation		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Central hypoventilation syndrome, congenital, MIM# 209880				14532329		False	2	0;100;0	1.5	True		ENSG00000139352	ENSG00000139352	HGNC:738													
LBX1	gene	LBX1	Expert Review;Expert Review Amber	Central Hypoventilation		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Central hypoventilation syndrome, congenital, 3, MIM#619483				30487221		False	2	0;100;0	1.5	True		ENSG00000138136	ENSG00000138136	HGNC:16960