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
FAT4	gene	FAT4	Australian Genomics Health Alliance Brain Malformation Flagship;Expert Review Amber;Victorian Clinical Genetics Services	Periventricular Grey Matter Heterotopia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Van Maldergem syndrome 2, MIM# 615546			Grey matter heterotopia;HP:0002282	22473091;24056717		False	2	0;100;0	1.2	True		ENSG00000196159	ENSG00000196159	HGNC:23109													
KAT6B	gene	KAT6B	Expert Review Amber;Literature	Periventricular Grey Matter Heterotopia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	SBBYSS syndrome MIM #603736;Genitopatellar syndrome MIM #606170			Grey matter heterotopia;HP:0002282	32424177;23236640		False	2	0;100;0	1.2	True		ENSG00000156650	ENSG00000156650	HGNC:17582