ClinVar for Gene (Select 126806240) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154674	GRCh38/hg38 2p14(chr2:67161296-67998206)x1	ETAA1, HHC2:066644 +11 more	Copy number loss	See cases	GUncertain significance
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	LOC129934199, LOC129934200 +2457 more	Copy number gain	See cases	GBenign
Select item 152020	GRCh38/hg38 2p14-13.3(chr2:64587095-69876311)x1	AAK1, ACTR2 +216 more	Copy number loss	See cases	GLikely pathogenic
Select item 146814	GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3	C2orf74, CCT4 +768 more	Copy number gain	See cases	GPathogenic
Select item 58872	GRCh38/hg38 2p14(chr2:66239485-67988719)x3	ETAA1, HCNR606 +40 more	Copy number gain	See cases	GUncertain significance

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