Related gene-specific medical variations for Gene (Select 50859) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808805	GRCh37/hg19 4q32.3(chr4:167428990-167860888)x3	SPOCK3	Copy number gain	not provided	GUncertain significance
Select item 1341239	GRCh37/hg19 4q32.3(chr4:168034701-168115705)x1	SPOCK3	Copy number loss	not provided	GUncertain significance
Select item 980707	GRCh37/hg19 4q32.3(chr4:167817512-168996168)x1	SPOCK3	Copy number loss	not provided	GUncertain significance
Select item 814626	GRCh37/hg19 4q32.3(chr4:167490481-167693089)x3	SPOCK3	Copy number gain	not provided	GUncertain significance
Select item 443420	GRCh37/hg19 4q32.3(chr4:167634638-168841223)x3	SPOCK3	Copy number gain	See cases	GLikely benign

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