Related gene-specific medical variations for Gene (Select 137868) - ClinVar - NCBI

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Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808738	GRCh37/hg19 8p22(chr8:13975474-14321653)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 980308	GRCh37/hg19 8p22(chr8:13560318-14140093)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 980306	GRCh37/hg19 8p22(chr8:13933532-14395725)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 815102	GRCh37/hg19 8p22(chr8:14687209-15239240)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 815101	GRCh37/hg19 8p22(chr8:14346801-14848001)x3	SGCZ	Copy number gain	not provided	GLikely benign
Select item 815100	GRCh37/hg19 8p22(chr8:13933532-14044132)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 688881	GRCh37/hg19 8p22(chr8:13845508-13975474)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 688613	GRCh37/hg19 8p22(chr8:13815152-14149245)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 563495	GRCh37/hg19 8p22(chr8:14749732-15306611)x3	SGCZ	Copy number gain	not provided	GLikely benign
Select item 563450	GRCh37/hg19 8p22(chr8:14104767-14299171)x1	SGCZ	Copy number loss	not provided	GUncertain significance
Select item 443061	GRCh37/hg19 8p22(chr8:13752510-14660057)x3	SGCZ	Copy number gain	See cases	GUncertain significance
Select item 152379	GRCh38/hg38 8p22(chr8:14047934-14103793)x3	SGCZ	Copy number gain	See cases	GBenign
Select item 151537	GRCh38/hg38 8p22(chr8:14940111-14976577)x3	SGCZ	Copy number gain	See cases	GBenign
Select item 145248	GRCh38/hg38 8p22(chr8:14714802-14757672)x1	SGCZ	Copy number loss	See cases	GBenign