"GeneDx"[submitter] AND "LOC123464484"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	LOC123453201, LOC123453202 +1450 more	Copy number gain	See cases	GPathogenic
Select item 57984	GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3	LOC132088897, LOC132088898 +1201 more	Copy number gain	See cases	GPathogenic
Select item 57868	GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1	MIR944, MUC20 +557 more	Copy number loss	See cases	GPathogenic
Select item 57870	GRCh38/hg38 3q27.3-29(chr3:187446231-195029133)x1	ATP13A3, ATP13A3-DT +226 more	Copy number loss	See cases	GPathogenic
Select item 145885	GRCh38/hg38 3q28(chr3:190075909-190254725)x1	LOC123464484, LOC126806907 +6 more	Copy number loss	See cases	GLikely benign
Select item 1217208	NM_018192.3(P3H2):c.-187G>A	LOC123464484, P3H2	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar