"GeneDx"[submitter] AND "LOC121815958"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58776	GRCh38/hg38 10q23.33-24.2(chr10:92626680-97755102)x1	LOC105378448, LOC107195252 +245 more	Copy number loss	See cases	GPathogenic
Select item 58777	GRCh38/hg38 10q23.33-24.32(chr10:93181201-101356779)x1	LOC130004555, LOC130004556 +375 more	Copy number loss	See cases	GPathogenic
Select item 59401	GRCh38/hg38 10q24.1(chr10:95606298-95966000)x1	C10orf131, CC2D2B +24 more	Copy number loss	See cases	GUncertain significance
Select item 683043	NM_002860.4(ALDH18A1):c.1923+305_1923+306insT	ALDH18A1, LOC121815958	Insertion (intron variant)	not provided	GBenign
Select item 683040	NM_002860.4(ALDH18A1):c.1923+303_1923+304insCG	ALDH18A1, LOC121815958	Insertion (intron variant)	not provided	GBenign
Select item 683039	NM_002860.4(ALDH18A1):c.1923+302_1923+303insTC	ALDH18A1, LOC121815958	Insertion (intron variant)	not provided	GBenign
Select item 683038	NM_002860.4(ALDH18A1):c.1923+299A>T	ALDH18A1, LOC121815958	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar