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
CSF3R	gene	CSF3R	Expert list;Expert Review Red;Radboud University Medical Center, Nijmegen	Congenital neutropaenia	Primary immunodeficiency disorders	Haematological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neutrophilia, hereditary, 162830;Severe congenital neutropenic						False	1	50;0;50	1.24	True		ENSG00000119535	ENSG00000119535	HGNC:2439													
FCGR3B	gene	FCGR3B	Expert Review Red;Radboud University Medical Center, Nijmegen	Congenital neutropaenia	Primary immunodeficiency disorders	Haematological disorders	Unknown	Neutropenia,alloimmuneneonatal						False	1	0;0;100	1.24	True		ENSG00000162747	ENSG00000162747	HGNC:3620													
GATA1	gene	GATA1	Expert Review Red;UKGTN	Congenital neutropaenia	Primary immunodeficiency disorders	Haematological disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835						False	1	0;0;100	1.24	True		ENSG00000102145	ENSG00000102145	HGNC:4170													
RAC2	gene	RAC2	Expert Review Red;Radboud University Medical Center, Nijmegen	Congenital neutropaenia	Primary immunodeficiency disorders	Haematological disorders	Unknown	Neutrophil immunodeficiency syndrome, 608203						False	1	0;0;100	1.24	True		ENSG00000128340	ENSG00000128340	HGNC:9802