PLCH1-AS2[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145614	GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	LOC115995524, LOC115995525 +2647 more	Copy number gain	See cases	GPathogenic
Select item 57982	GRCh38/hg38 3q24-26.32(chr3:147442566-178522531)x3	LOC129937936, LOC129937937 +631 more	Copy number gain	See cases	GPathogenic
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	LOC123453201, LOC123453202 +1450 more	Copy number gain	See cases	GPathogenic
Select item 150609	GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	LOC129938169, LOC129938170 +1318 more	Copy number gain	See cases	GPathogenic
Select item 144842	GRCh38/hg38 3q25.31(chr3:155388702-155490802)x3	LOC123230398, PLCH1 +2 more	Copy number gain	See cases	GBenign
Select item 788519	NM_014996.4(PLCH1):c.2620-461A>T	PLCH1, PLCH1-AS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

ClinVar