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
BRPF1	gene	BRPF1	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder with dysmorphic facies and ptosis, MIM# 617333				36117209;27939640;38346666		False	3	100;0;0	1.27	True		ENSG00000156983	ENSG00000156983	HGNC:14255													
CDK13	gene	CDK13	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder, MIM# 617360				32345733;36599938		False	3	100;0;0	1.27	True		ENSG00000065883	ENSG00000065883	HGNC:1733													
CHD3	gene	CHD3	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Snijders Blok-Campeau syndrome MIM#618205				PMID: 30397230;38366112;35346573		False	3	100;0;0	1.27	True		ENSG00000170004	ENSG00000170004	HGNC:1918													
DDX3X	gene	DDX3X	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Intellectual developmental disorder, X-linked syndromic, Snijders Blok type, MIM# 300958				32345733;36117209;37904618		False	3	100;0;0	1.27	True		ENSG00000215301	ENSG00000215301	HGNC:2745													
EBF3	gene	EBF3	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypotonia, ataxia, and delayed development syndrome, MIM# 617330				32345733;28017372		False	3	100;0;0	1.27	True		ENSG00000108001	ENSG00000108001	HGNC:19087													
FOXP2	gene	FOXP2	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Speech-language disorder-1, MIM# 602081				PMID: 11586359;36328423;38366112		False	3	100;0;0	1.27	True		ENSG00000128573	ENSG00000128573	HGNC:13875													
KAT6A	gene	KAT6A	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arboleda-Tham syndrome, MIM# 616268				35892268;38366112;30245513		False	3	100;0;0	1.27	True		ENSG00000083168	ENSG00000083168	HGNC:13013													
SETBP1	gene	SETBP1	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder, autosomal dominant 29, MIM# 616078				29463886;33907317		False	3	100;0;0	1.27	True		ENSG00000152217	ENSG00000152217	HGNC:15573													
SETD1A	gene	SETD1A	Expert list;Expert Review;Expert Review Green	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder with speech impairment and dysmorphic facies, MIM# 619056				29463886;32346159		False	3	100;0;0	1.27	True		ENSG00000099381	ENSG00000099381	HGNC:29010