Related gene-specific medical variations for Gene (Select 80868) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 157004	NR_001317.3(HCG4B):n.-1429_25883del	HCG4B	Deletion	Small for gestational age	Gnot provided
Select item 147228	GRCh38/hg38 6p22.1(chr6:29887122-29928906)x1	HCG4B	Copy number loss	See cases	GBenign
Select item 147103	GRCh38/hg38 6p22.1(chr6:29887122-29934508)x1	HCG4B	Copy number loss	See cases	GBenign

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