"GeneDx"[submitter] AND "GYPC"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60185	GRCh38/hg38 2q14.3(chr2:121824798-128870804)x1	AMMECR1L, BIN1 +121 more	Copy number loss	See cases	GPathogenic
Select item 60186	GRCh38/hg38 2q14.3(chr2:122324343-128371704)x1	LOC115945190, LOC120961783 +101 more	Copy number loss	See cases	GPathogenic
Select item 58902	GRCh38/hg38 2q14.3(chr2:125574480-126753377)x3	GYPC, LINC01889 +11 more	Copy number gain	See cases	GUncertain significance
Select item 1242153	NC_000002.12:g.126656040G>A	GYPC, LOC129934705	Single nucleotide variant	not provided	GBenign
Select item 1257983	NM_002101.5(GYPC):c.50-68G>A	GYPC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257288	NM_002101.5(GYPC):c.191-262del	GYPC	Deletion (intron variant)	not provided	GBenign
Select item 1262546	NM_002101.5(GYPC):c.191-261A>C	GYPC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294938	NM_002101.5(GYPC):c.191-221C>T	GYPC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238066	NM_002101.5(GYPC):c.191-136C>T	GYPC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258136	NM_002101.5(GYPC):c.191-43G>A	GYPC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295027	NM_002101.5(GYPC):c.333A>C (p.Gly111=)	GYPC	Single nucleotide variant (synonymous variant)	not provided	GBenign