ClinVar for Gene (Select 100653233) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155524	GRCh38/hg38 7p11.2(chr7:57144128-57966167)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	GUncertain significance
Select item 155365	GRCh38/hg38 7p11.2(chr7:57233248-57966167)x3	LOC132089552, MIR3147 +2 more	Copy number gain	See cases	GLikely benign
Select item 155343	GRCh38/hg38 7p11.2(chr7:57166206-57819147)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	GUncertain significance
Select item 155070	GRCh38/hg38 7p11.2(chr7:57193415-57846998)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 155051	GRCh38/hg38 7p11.2(chr7:57193415-57821414)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	GLikely benign
Select item 154139	GRCh38/hg38 7p11.2(chr7:57193415-57859810)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	GLikely benign
Select item 153576	GRCh38/hg38 7p11.2(chr7:57120582-57966167)x1	LOC105375297, LOC132089552 +4 more	Copy number loss	See cases	GUncertain significance
Select item 153523	GRCh38/hg38 7p11.2(chr7:57193415-57863780)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 153486	GRCh38/hg38 7p11.2(chr7:57193415-57864134)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 153217	GRCh38/hg38 7p11.2(chr7:57193415-57818047)x3	LOC105375297, LOC132089552 +3 more	Copy number gain	See cases	GLikely benign
Select item 152303	GRCh38/hg38 7p11.2(chr7:57233248-57965704)x3	LOC132089552, MIR3147 +2 more	Copy number gain	See cases	GUncertain significance
Select item 151312	GRCh38/hg38 7p11.2(chr7:57130102-57649953)x1	LOC105375297, LOC132089552 +4 more	Copy number loss	See cases	GUncertain significance
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CCDC146, CCDC201 +4735 more	Copy number loss	See cases	GPathogenic
Select item 59682	GRCh38/hg38 7p12.1-q11.22(chr7:53274059-68576213)x3	ASL, CCT6A +228 more	Copy number gain	See cases	GPathogenic
Select item 59680	GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3	LOC129389795, LOC129389796 +636 more	Copy number gain	See cases	GPathogenic
Select item 59596	GRCh38/hg38 7p12.1-11.2(chr7:52192528-57823293)x3	CCT6A, CHCHD2 +107 more	Copy number gain	See cases	GUncertain significance
Select item 58866	GRCh38/hg38 7p12.1-11.2(chr7:52114454-57434735)x1	CCT6A, CHCHD2 +107 more	Copy number loss	See cases	GUncertain significance