"GeneDx"[submitter] AND "PCDH9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58260	GRCh38/hg38 13q21.32(chr13:65645518-66626184)x3	LINC01052, LOC110120945 +7 more	Copy number gain	See cases	GUncertain significance
Select item 152622	GRCh38/hg38 13q21.32(chr13:66529771-66592227)x1	LOC124900161, PCDH9	Copy number loss	See cases	Gconflicting data from submitters
Select item 145868	GRCh38/hg38 13q21.32(chr13:66641542-66825751)x1	PCDH9, PCDH9-AS2	Copy number loss	See cases	GLikely benign
Select item 145848	GRCh38/hg38 13q21.32(chr13:66733239-66832341)x1	PCDH9, PCDH9-AS2	Copy number loss	See cases	GLikely benign
Select item 145266	GRCh38/hg38 13q21.32(chr13:66753669-66774687)x1	PCDH9	Copy number loss	See cases	GBenign
Select item 1338957	NM_203487.3(PCDH9):c.2154G>C (p.Val718=)	PCDH9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic

ClinVar