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
CCND2	gene	CCND2	Expert list;Expert Review Amber;NHS GMS	Mosaic brain disorders - deep sequencing		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3, OMIM:615938				24705253		False	2	33;33;33	0.149	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000118971	ENSG00000118971	HGNC:1583													
NPRL2	gene	NPRL2	Expert list;Expert Review Amber;NHS GMS	Mosaic brain disorders - deep sequencing		Neurology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Epilepsy, familial focal, with variable foci 2, OMIM:617116;Focal cortical dysplasia				26505888;31625153;30093711		False	2	50;50;0	0.149	False		ENSG00000114388	ENSG00000114388	HGNC:24969