ClinVar for Gene (Select 79470) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2641539	NM_001005567.3(OR51B5):c.-359-55947T>A	OR51J1, OR51B5	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2641538	NM_001005567.3(OR51B5):c.-359-55753G>A	OR51B5, OR51J1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 151263	GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3	LOC130005128, LOC130005129 +723 more	Copy number gain	See cases	GPathogenic
Select item 144515	GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3	CHID1, CHRNA10 +917 more	Copy number gain	See cases	GPathogenic

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