Related gene-specific medical variations for Gene (Select 283914) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 161009	GRCh38/hg38 16p11.2-11.1(chr16:35247671-35492978)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 150423	GRCh38/hg38 16p11.2-11.1(chr16:35247701-35493160)x3	LINC01566	Copy number gain	See cases	GBenign/Likely benign
Select item 147543	GRCh38/hg38 16p11.2-11.1(chr16:35247671-35448077)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 147194	GRCh38/hg38 16p11.1(chr16:35390780-35513188)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 147160	GRCh38/hg38 16p11.1(chr16:35305312-35375014)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 147126	GRCh38/hg38 16p11.2-11.1(chr16:35283467-35467582)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 146968	GRCh38/hg38 16p11.2-11.1(chr16:35247701-35492950)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 146745	GRCh38/hg38 16p11.2-11.1(chr16:35247701-35492994)x1	LINC01566	Copy number loss	See cases	GBenign
Select item 146744	GRCh38/hg38 16p11.2-11.1(chr16:35247701-35492994)x3	LINC01566	Copy number gain	See cases	GBenign/Likely benign
Select item 146153	GRCh38/hg38 16p11.2-11.1(chr16:35247471-35493121)x3	LINC01566	Copy number gain	See cases	GBenign
Select item 32463	GRCh38/hg38 16p11.2-11.1(chr16:35247671-35492978)x3	LINC01566	Copy number gain	See cases	GBenign