"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "DCP1B"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 776685	NM_152640.5(DCP1B):c.1701G>A (p.Pro567=)	DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 712109	NM_152640.5(DCP1B):c.1629C>T (p.Ser543=)	DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 781059	NM_152640.5(DCP1B):c.1151G>A (p.Arg384His)	DCP1B (R384H)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 773020	NM_152640.5(DCP1B):c.902G>C (p.Ser301Thr)	DCP1B (S301T)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2427496	NC_000012.11:g.(?_862732)_(2800365_?)dup	ADIPOR2, CACNA1C +8 more	Duplication	not provided	GUncertain significance
Select item 2423370	NC_000012.11:g.(?_2016586)_(2558301_?)dup	CACNA1C, CACNA2D4 +1 more	Duplication	Long QT syndrome	GUncertain significance
Select item 2423369	NC_000012.11:g.(?_1949885)_(2764424_?)dup	CACNA1C, CACNA2D4 +1 more	Duplication	Long QT syndrome	GUncertain significance
Select item 1434649	NC_000012.11:g.(?_1949885)_(2229616_?)dup	CACNA1C, CACNA2D4 +1 more	Duplication	not provided	GUncertain significance
Select item 833161	NC_000012.12:g.(?_1909906)_(2556977_?)dup	DCP1B, CACNA1C +1 more	Duplication	not provided	GUncertain significance

ClinVar