"GeneDx"[submitter] AND "KIAA0825"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58096	GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3	ATG10, ATP6AP1L +691 more	Copy number gain	See cases	GPathogenic
Select item 59664	GRCh38/hg38 5q14.3-21.2(chr5:89081352-104687248)x1	ADGRV1, ARB2A +275 more	Copy number loss	See cases	GPathogenic
Select item 59667	GRCh38/hg38 5q14.3-15(chr5:91386552-98365880)x1	ARB2A, ARRDC3-AS1 +147 more	Copy number loss	See cases	GPathogenic
Select item 59670	GRCh38/hg38 5q15(chr5:93598243-94237822)x1	ARB2A, KIAA0825 +7 more	Copy number loss	See cases	GPathogenic
Select item 152919	GRCh38/hg38 5q15(chr5:93812177-94727962)x1	ARB2A, KIAA0825 +9 more	Copy number loss	See cases	GUncertain significance
Select item 599402	NM_001145678.3(KIAA0825):c.2173A>T (p.Lys725Ter)	KIAA0825 (K725*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance

ClinVar