"GeneDx"[submitter] AND "LOC130064984"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 507762	NM_001256849.1(POLD1):c.-51G>C	LOC130064984, POLD1	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 380428	NM_001256849.1(POLD1):c.-51G>A	LOC130064984, POLD1	Single nucleotide variant (5 prime UTR variant)	Colorectal cancer, susceptibility to, 10 +2 more	GBenign/Likely benign
Select item 423128	NM_002691.4(POLD1):c.-44_-36delinsACACGGCGA	LOC130064984, POLD1	Indel (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 382308	NM_002691.4(POLD1):c.-32A>G	LOC130064984, POLD1	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign

ClinVar