Related gene-specific medical variations for Gene (Select 441308) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152002	GRCh38/hg38 8p23.3(chr8:137572-171006)x3	OR4F21	Copy number gain	See cases	GBenign
Select item 144945	GRCh38/hg38 8p23.3(chr8:137572-178199)x1	OR4F21	Copy number loss	See cases	GBenign
Select item 144944	GRCh38/hg38 8p23.3(chr8:137572-178199)x3	OR4F21	Copy number gain	See cases	GBenign

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