Related gene-specific medical variations for Gene (Select 132430) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340676	GRCh37/hg19 4q28.3(chr4:134983908-135303785)x3	PABPC4L	Copy number gain	not provided	GUncertain significance
Select item 154838	GRCh38/hg38 4q28.3(chr4:134022175-134259030)x1	PABPC4L	Copy number loss	See cases	GLikely benign
Select item 147849	GRCh38/hg38 4q28.3(chr4:134022081-134259014)x1	PABPC4L	Copy number loss	See cases	GBenign
Select item 146106	GRCh38/hg38 4q28.3(chr4:134021881-134259155)x1	PABPC4L	Copy number loss	See cases	GBenign