"GeneDx"[submitter] AND "LOC123493308"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59608	GRCh38/hg38 5q11.1-11.2(chr5:50462100-55862985)x1	ARL15, CCNO +96 more	Copy number loss	See cases	GPathogenic
Select item 1278187	NM_021147.5(CCNO):c.-65G>T	CCNO, LOC123493308	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1263712	NC_000005.10:g.55233630C>G	CCNO, LOC123493308	Single nucleotide variant	not provided	GBenign
Select item 1275363	NC_000005.10:g.55233776G>A	CCNO, LOC123493308	Single nucleotide variant	not provided	GBenign
Select item 1272415	NC_000005.10:g.55233802A>C	CCNO, LOC123493308	Single nucleotide variant	not provided	GBenign
Select item 1221093	NC_000005.10:g.55233874GTCACTGCGGAGCCCGG[1]	CCNO, LOC123493308	Microsatellite	not provided	GBenign

ClinVar