ClinVar for Gene (Select 80868) - ClinVar

	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 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	CYP39A1, DAAM2 +2577 more	Copy number gain	See cases	GPathogenic
Select item 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	LOC129995913, LOC129995914 +1340 more	Copy number gain	See cases	GPathogenic
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
Select item 147086	GRCh38/hg38 6p22.1(chr6:29887122-29969806)x1	HCG4B, HLA-A +1 more	Copy number loss	See cases	GBenign

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