Related gene-specific medical variations for Gene (Select 255403) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340278	GRCh37/hg19 4p16.3(chr4:146604-259488)x3	ZNF718	Copy number gain	not provided	GLikely benign
Select item 814525	GRCh37/hg19 4p16.3(chr4:102156-249924)x3	ZNF718	Copy number gain	not provided	GLikely benign
Select item 151690	GRCh38/hg38 4p16.3(chr4:135972-227660)x3	ZNF718	Copy number gain	See cases	GBenign
Select item 145388	GRCh38/hg38 4p16.3(chr4:149300-191519)x1	ZNF718	Copy number loss	See cases	GBenign
Select item 144599	GRCh38/hg38 4p16.3(chr4:162315-180719)x3	ZNF718	Copy number gain	See cases	GBenign
Select item 144155	GRCh38/hg38 4p16.3(chr4:153787-191636)x1	ZNF718	Copy number loss	See cases	GBenign

ClinVar