"GeneDx"[submitter] AND "LOC113875008"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145168	GRCh38/hg38 Xq21.1-28(chrX:78605009-156016560)x1	LOC125467786, LOC125467787 +1203 more	Copy number loss	See cases	GPathogenic
Select item 58668	GRCh38/hg38 Xq25-28(chrX:123731372-155687381)x3	MIR2114, MIR224 +718 more	Copy number gain	See cases	GPathogenic
Select item 58669	GRCh38/hg38 Xq25-26.2(chrX:128395951-132383344)x2	AIFM1, APLN +127 more	Copy number gain	See cases	GPathogenic
Select item 1291490	NC_000023.11:g.129540157C>T	LOC113875008, OCRL	Single nucleotide variant	not provided	GBenign
Select item 1259336	NC_000023.11:g.129540176C>T	LOC113875008, OCRL	Single nucleotide variant	not provided	GBenign
Select item 423653	NM_000276.4(OCRL):c.25G>A (p.Ala9Thr)	LOC113875008, OCRL (A9T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar