"GeneDx"[submitter] AND "C22orf15"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1238466	NC_000022.11:g.23765747C>T	C22orf15, CHCHD10 (T156I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1240465	NC_000022.11:g.23765813C>G	C22orf15, CHCHD10	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 253981	GRCh37/hg19 22q11.23(chr22:23950632-24276233)x4	C22orf15, DERL3 +9 more	Copy number gain	See cases	GUncertain significance
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 253499	GRCh37/hg19 22q11.22-11.23(chr22:22988879-24276233)x3	CHCHD10, RAB36 +17 more	Copy number gain	See cases	GPathogenic
Select item 253485	GRCh37/hg19 22q11.22-11.23(chr22:22976696-25053311)x3	GSTT2B, VPREB3 +32 more	Copy number gain	See cases	GPathogenic
Select item 253473	GRCh37/hg19 22q11.1-12.1(chr22:16054691-27296513)x3	ADA2, ADORA2A +135 more	Copy number gain	See cases	GPathogenic
Select item 253435	GRCh37/hg19 22q11.22-11.23(chr22:23258229-25046803)x3	RSPH14, SNRPD3 +29 more	Copy number gain	See cases	GPathogenic

ClinVar