Related gene-specific medical variations for Gene (Select 1350) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809474	GRCh37/hg19 5q14.3(chr5:85849576-86109647)x3	COX7C	Copy number gain	not provided	GUncertain significance
Select item 686615	GRCh37/hg19 5q14.3(chr5:85607233-86539904)x3	COX7C	Copy number gain	not provided	GUncertain significance
Select item 395337	GRCh37/hg19 5q14.3(chr5:85914403-86096388)x3	COX7C	Copy number gain	See cases	GLikely benign

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