ClinVar for Gene (Select 115801414) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 147192	GRCh38/hg38 14q11.2(chr14:19193116-19344465)x1	LINC01297, LINC01297-DUXAP10-NBEAP6 +1 more	Copy number loss	See cases	GBenign
Select item 147182	GRCh38/hg38 14q11.2(chr14:18907993-19415424)x1	LINC01296, LINC01297 +6 more	Copy number loss	See cases	GBenign
Select item 147131	GRCh38/hg38 14q11.2(chr14:18907993-19433294)x3	LINC01296, LINC01297 +7 more	Copy number gain	See cases	GBenign
Select item 147071	GRCh38/hg38 14q11.2(chr14:18907993-19298380)x3	LINC01296, LINC01297-DUXAP10-NBEAP6 +3 more	Copy number gain	See cases	GBenign
Select item 146998	GRCh38/hg38 14q11.2(chr14:18698325-19967729)x1	LINC01296, LINC01297 +15 more	Copy number loss	See cases	GBenign
Select item 146977	GRCh38/hg38 14q11.2(chr14:18907993-19386058)x1	LINC01296, LINC01297 +5 more	Copy number loss	See cases	GBenign
Select item 146963	GRCh38/hg38 14q11.2(chr14:18600315-19967729)x1	LINC01296, LINC01297 +17 more	Copy number loss	See cases	GBenign
Select item 146947	GRCh38/hg38 14q11.2(chr14:18600315-19946044)x3	LINC01296, LINC01297 +17 more	Copy number gain	See cases	GBenign
Select item 146936	GRCh38/hg38 14q11.2(chr14:18658128-19967729)x1	LINC01296, LINC01297 +15 more	Copy number loss	See cases	GBenign
Select item 58303	GRCh38/hg38 14q11.2(chr14:18907993-19498584)x3	LINC01296, LINC01297 +7 more	Copy number gain	See cases	GUncertain significance