Related gene-specific medical variations for Gene (Select 154215) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685040	GRCh37/hg19 6q22.31(chr6:124918580-125201001)x4	NKAIN2	Copy number gain	not provided	GUncertain significance
Select item 980782	GRCh37/hg19 6q22.31(chr6:124632709-124755323)x1	NKAIN2	Copy number loss	not provided	GUncertain significance
Select item 684480	Single allele	NKAIN2	Duplication	not provided	Gnot provided
Select item 563232	GRCh37/hg19 6q22.31(chr6:124691423-124984989)x3	NKAIN2	Copy number gain	not provided	GUncertain significance
Select item 563231	GRCh37/hg19 6q22.31(chr6:124496938-125189118)x3	NKAIN2	Copy number gain	not provided	GUncertain significance
Select item 393891	GRCh37/hg19 6q22.31(chr6:124373571-124463314)x1	NKAIN2	Copy number loss	See cases	GUncertain significance
Select item 157026	NM_001040214.2(NKAIN2):c.55-187304_55-129556dup	NKAIN2	Duplication	Small for gestational age	Gnot provided
Select item 157025	NM_001040214.2(NKAIN2):c.55-199612_55-129556dup	NKAIN2	Duplication	Normal pregnancy	Gnot provided
Select item 58444	GRCh38/hg38 6q22.31(chr6:124116341-124499647)x1	NKAIN2	Copy number loss	See cases	GPathogenic

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