ClinVar for Gene (Select 106146148) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150866	GRCh38/hg38 22p11.2-q11.1(chr22:10874347-15903760)x4	LOC102723769, OR11H1 +3 more	Copy number gain	See cases	GPathogenic
Select item 148896	GRCh38/hg38 22p11.2-q11.1(chr22:10874347-15903760)x1	LOC102723769, OR11H1 +3 more	Copy number loss	See cases	GLikely pathogenic
Select item 148560	GRCh38/hg38 22p11.2-q11.1(chr22:10874347-15903760)x3	LOC102723769, OR11H1 +3 more	Copy number gain	See cases	GPathogenic
Select item 148188	GRCh38/hg38 22q11.1-11.21(chr22:10874347-15903760)x3	LOC102723769, OR11H1 +3 more	Copy number gain	See cases	GPathogenic
Select item 59276	GRCh38/hg38 22q11.1-11.21(chr22:11119188-16489297)x3	LOC102723769, LOC129391256 +4 more	Copy number gain	See cases	GPathogenic
Select item 59275	GRCh38/hg38 22q11.1-11.21(chr22:11121452-18167952)x3	CECR7, GAB4 +116 more	Copy number gain	See cases	GPathogenic

ClinVar