"GeneDx"[submitter] AND "LOC130059225"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58632	GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3	LOC130059197, LOC130059198 +575 more	Copy number gain	See cases	GPathogenic
Select item 59493	GRCh38/hg38 16q21-22.1(chr16:64311275-68062011)x1	ACD, AGRP +217 more	Copy number loss	See cases	GPathogenic
Select item 59494	GRCh38/hg38 16q22.1(chr16:66694180-67865445)x1	ACD, AGRP +155 more	Copy number loss	See cases	GPathogenic
Select item 1804577	NC_000016.10:g.67660837T>C	ACD, LOC130059225	Single nucleotide variant	not provided	GLikely benign
Select item 1707123	NC_000016.10:g.67660909A>G	ACD, LOC130059225	Single nucleotide variant	not provided	GLikely benign
Select item 1267204	NC_000016.10:g.67660959_67660963dup	ACD, LOC130059225	Duplication	not provided	GBenign

ClinVar