"GeneDx"[submitter] AND "GPR12"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59853	GRCh38/hg38 13q11-13.3(chr13:18676442-37656039)x3	LOC130009419, LOC130009420 +567 more	Copy number gain	See cases	GPathogenic
Select item 59861	GRCh38/hg38 13q12.11-12.3(chr13:18958091-31090460)x3	LOC130009490, LOC130009491 +416 more	Copy number gain	See cases	GPathogenic
Select item 1226768	NM_005288.4(GPR12):c.*124T>C	GPR12	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1279212	NM_005288.4(GPR12):c.-15-45A>G	GPR12	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291579	NM_005288.4(GPR12):c.-15-105A>G	GPR12	Single nucleotide variant (intron 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