Related gene-specific medical variations for Gene (Select 92293) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 974760	NC_000012.11:g.128208742_128917555dup	TMEM132C	Duplication	Megacolon	GUncertain significance
Select item 563966	GRCh37/hg19 12q24.32(chr12:127813228-128908855)x3	TMEM132C	Copy number gain	not provided	GLikely benign
Select item 563962	GRCh37/hg19 12q24.32(chr12:128273417-129100970)x3	TMEM132C	Copy number gain	not provided	GUncertain significance
Select item 443853	GRCh37/hg19 12q24.32(chr12:128222409-128912350)x3	TMEM132C	Copy number gain	See cases	GUncertain significance
Select item 443111	GRCh37/hg19 12q24.32(chr12:127556405-128910967)x4	TMEM132C	Copy number gain	See cases	GLikely benign
Select item 394357	GRCh37/hg19 12q24.32(chr12:128385044-128906983)x3	TMEM132C	Copy number gain	See cases	GLikely benign

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