"GeneDx"[submitter] AND "LOC130004108"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58726	GRCh38/hg38 10q21.1-22.2(chr10:58436466-74415216)x1	LOC129390190, LOC129390191 +610 more	Copy number loss	See cases	GPathogenic
Select item 58745	GRCh38/hg38 10q22.1-22.2(chr10:72720628-75612374)x1	LOC130004132, LOC130004133 +150 more	Copy number loss	See cases	GPathogenic
Select item 684057	NM_014000.2(VCL):c.-386A>G	LOC130004108, VCL	Single nucleotide variant	not provided	GBenign
Select item 684060	NM_014000.2(VCL):c.-264A>G	LOC130004108, VCL	Single nucleotide variant	not provided	GBenign
Select item 1205590	NC_000010.11:g.73998025C>T	LOC130004108, VCL	Single nucleotide variant	not provided	GLikely benign
Select item 1188273	NC_000010.11:g.73998048G>A	LOC130004108, VCL	Single nucleotide variant	not provided	GLikely benign

ClinVar