"GeneDx"[submitter] AND "LOC126862606"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151500	GRCh38/hg38 17q22-23.1(chr17:57418806-59735464)x1	C17orf47, CCDC182 +168 more	Copy number loss	See cases	GPathogenic
Select item 152571	GRCh38/hg38 17q22(chr17:58940516-59008749)x3	LOC126862606, LOC129390904 +2 more	Copy number gain	See cases	GLikely benign
Select item 1188455	NM_015294.6(TRIM37):c.2812+129dup	LOC126862606, TRIM37	Duplication (intron variant)	not provided	GLikely benign
Select item 1195503	NM_015294.6(TRIM37):c.2812+143del	LOC126862606, TRIM37	Deletion (intron variant)	not provided	GLikely benign
Select item 1206427	NM_015294.6(TRIM37):c.2812+68T>G	LOC126862606, TRIM37	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 265280	NM_015294.6(TRIM37):c.2696-2A>G	LOC126862606, TRIM37	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely pathogenic

ClinVar