Related gene-specific medical variations for Gene (Select 64067) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807987	GRCh37/hg19 14q13.1(chr14:33656354-34157207)x1	NPAS3	Copy number loss	not provided	GUncertain significance
Select item 1341281	GRCh37/hg19 14q13.1(chr14:33656353-34162087)x1	NPAS3	Copy number loss	not provided	GUncertain significance
Select item 1340713	GRCh37/hg19 14q13.1(chr14:33766967-34010728)x1	NPAS3	Copy number loss	not provided	GUncertain significance
Select item 980481	GRCh37/hg19 14q13.1(chr14:33463166-33998038)x1	NPAS3	Copy number loss	not provided	GLikely benign
Select item 545162	NC_000014.9:g.(?_33318664)_(33378429_?)del	NPAS3	Deletion	Schizophrenia	GLikely pathogenic
Select item 524172	t(12;14)(q14;q13)dn	LIN7A, NPAS3	Translocation	not provided	GLikely pathogenic
Select item 442561	GRCh37/hg19 14q13.1(chr14:34017469-34207276)x3	NPAS3	Copy number gain	See cases	GUncertain significance
Select item 152789	GRCh38/hg38 14q13.1(chr14:33194658-33238149)x3	NPAS3	Copy number gain	See cases	GUncertain significance

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