"GeneDx"[submitter] AND "LOC126807284"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59557	GRCh38/hg38 5p15.33(chr5:22149-3556942)x1	AHRR, BRD9 +194 more	Copy number loss	See cases	GPathogenic
Select item 59578	GRCh38/hg38 5p15.33(chr5:37694-2913205)x1	LOC132090723, LOC132090724 +182 more	Copy number loss	See cases	GPathogenic
Select item 59577	GRCh38/hg38 5p15.33(chr5:37694-2746908)x1	AHRR, BRD9 +180 more	Copy number loss	See cases	GPathogenic
Select item 59601	GRCh38/hg38 5p15.33-15.32(chr5:54839-5603401)x1	ADAMTS16, ADAMTS16-DT +226 more	Copy number loss	See cases	GPathogenic
Select item 1233356	NM_001044.5(SLC6A3):c.1599+339_1599+345del	LOC126807284, SLC6A3	Deletion (intron variant)	not provided	GBenign
Select item 1272852	NM_001044.5(SLC6A3):c.1599+267G>T	LOC126807284, SLC6A3	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar