"GeneDx"[submitter] AND "LOC129931513"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60040	GRCh38/hg38 1q21.3-22(chr1:154575689-155292901)x1	LOC129931527, LOC129931528 +91 more	Copy number loss	See cases	GPathogenic
Select item 1215236	NM_001025107.3(ADAR):c.-870-5705_-870-5704dup	ADAR, LOC129931513	Duplication (intron variant)	not provided	GLikely benign
Select item 1211470	NM_001025107.3(ADAR):c.-870-5704dup	ADAR, LOC129931513	Duplication (intron variant)	not provided	GLikely benign
Select item 1277075	NM_001025107.3(ADAR):c.-870-5704del	ADAR, LOC129931513	Deletion (intron variant)	not provided	GBenign
Select item 1252259	NM_001025107.3(ADAR):c.-870-5732G>A	ADAR, LOC129931513	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296014	NM_001025107.3(ADAR):c.-870-5793G>C	ADAR, LOC129931513	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar