Related gene-specific medical variations for Gene (Select 286319) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980352	GRCh37/hg19 9p21.3-21.2(chr9:25158495-25684180)x3	TUSC1	Copy number gain	not provided	GLikely benign
Select item 980345	GRCh37/hg19 9p21.2(chr9:25656156-25863777)x1	TUSC1	Copy number loss	not provided	GLikely benign
Select item 563666	GRCh37/hg19 9p21.3-21.2(chr9:25185518-26752060)x3	TUSC1	Copy number gain	not provided	GLikely benign
Select item 563640	GRCh37/hg19 9p21.3-21.2(chr9:25308250-25845456)x3	TUSC1	Copy number gain	not provided	GLikely benign
Select item 563603	GRCh37/hg19 9p21.3-21.2(chr9:25481660-25679189)x1	TUSC1	Copy number loss	not provided	GUncertain significance
Select item 146691	GRCh38/hg38 9p21.3-21.2(chr9:25548165-25702908)x1	TUSC1	Copy number loss	See cases	GUncertain significance

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