Related gene-specific medical variations for Gene (Select 158038) - ClinVar

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Links from Gene

Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685348	GRCh37/hg19 9p21.1(chr9:28698217-29061610)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 2685347	GRCh37/hg19 9p21.1(chr9:28257648-28585960)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 1809025	GRCh37/hg19 9p21.2-21.1(chr9:27780310-28605043)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 1808925	GRCh37/hg19 9p21.2-21.1(chr9:27670414-28070014)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 1340565	GRCh37/hg19 9p21.1(chr9:28905419-28981481)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 980342	GRCh37/hg19 9p21.1(chr9:28737913-29702414)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 980341	GRCh37/hg19 9p21.1(chr9:28937299-29198547)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 980340	GRCh37/hg19 9p21.1(chr9:29129023-29202522)x1	LINGO2	Copy number loss	not provided	GLikely benign
Select item 980339	GRCh37/hg19 9p21.1(chr9:28492136-28818016)x1	LINGO2	Copy number loss	not provided	GLikely benign
Select item 974737	NM_001258282.3(LINGO2):c.-228+12976_-227-20514del	LINGO2	Deletion (intron variant)	Megacolon	GUncertain significance
Select item 815258	GRCh37/hg19 9p21.1(chr9:28885984-29088636)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 815257	GRCh37/hg19 9p21.1(chr9:28620371-28975706)x1	LINGO2	Copy number loss	not provided	GLikely benign
Select item 815256	GRCh37/hg19 9p21.1(chr9:28183564-31526964)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 815255	GRCh37/hg19 9p21.1(chr9:28130036-28378182)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 815254	GRCh37/hg19 9p21.2-21.1(chr9:27745383-28346159)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 689254	GRCh37/hg19 9p21.1(chr9:28586142-28766607)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 689235	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 689184	GRCh37/hg19 9p21.1(chr9:28739852-28916553)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 689152	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 689134	GRCh37/hg19 9p21.1(chr9:28593228-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688944	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688928	GRCh37/hg19 9p21.1(chr9:28189976-28347399)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688923	GRCh37/hg19 9p21.1(chr9:29057538-29244165)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688776	GRCh37/hg19 9p21.1(chr9:28588574-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688673	GRCh37/hg19 9p21.1(chr9:28593228-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688668	GRCh37/hg19 9p21.1(chr9:28635167-28680869)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688656	GRCh37/hg19 9p21.1(chr9:28588574-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688565	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688454	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 688287	GRCh37/hg19 9p21.1(chr9:28513869-28812497)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688232	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688220	GRCh37/hg19 9p21.1(chr9:28593134-28766607)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688203	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688111	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688018	GRCh37/hg19 9p21.1(chr9:28586142-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 688012	GRCh37/hg19 9p21.1(chr9:28603176-28769160)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 687779	GRCh37/hg19 9p21.1(chr9:29122523-29244165)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 687692	GRCh37/hg19 9p21.1(chr9:28586142-28761784)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 686919	GRCh37/hg19 9p21.1(chr9:28975710-29298962)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 686910	GRCh37/hg19 9p21.1(chr9:28698216-28725108)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 686885	GRCh37/hg19 9p21.1(chr9:28689311-28738160)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 685666	GRCh37/hg19 9p21.1(chr9:29178486-29284164)x3	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 685520	GRCh37/hg19 9p21.1(chr9:28620371-28742801)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 685460	GRCh37/hg19 9p21.1(chr9:28673985-28824856)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 685319	GRCh37/hg19 9p21.1(chr9:28693056-28795502)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 685312	GRCh37/hg19 9p21.1(chr9:28588574-28766228)x1	LINGO2	Copy number loss	not provided	GUncertain significance
Select item 563615	GRCh37/hg19 9p21.1(chr9:28018586-28262531)x4	LINGO2	Copy number gain	not provided	GUncertain significance
Select item 441636	GRCh37/hg19 9p21.1(chr9:28427025-28725108)x1	LINGO2	Copy number loss	See cases	GUncertain significance
Select item 441590	GRCh37/hg19 9p21.1(chr9:28303003-28509732)x1	LINGO2	Copy number loss	See cases	GUncertain significance
Select item 441582	GRCh37/hg19 9p21.1(chr9:28543761-28848834)x1	LINGO2	Copy number loss	See cases	GLikely benign
Select item 441561	GRCh37/hg19 9p21.1(chr9:28174369-29604517)x3	LINGO2	Copy number gain	See cases	GLikely benign
Select item 221726	GRCh38/hg38 9p21.1(chr9:28195208-28336187)x1	LINGO2	Copy number loss	Premature ovarian failure	GBenign
Select item 157142	Single allele	LINGO2	Deletion	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 153482	GRCh38/hg38 9p21.1(chr9:28030643-28378184)x1	LINGO2	Copy number loss	See cases	GUncertain significance
Select item 152233	GRCh38/hg38 9p21.1(chr9:28082558-28648398)x3	LINGO2	Copy number gain	See cases	GLikely benign
Select item 144970	GRCh38/hg38 9p21.1(chr9:28191463-28320733)x1	LINGO2	Copy number loss	See cases	GBenign

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Links from Gene

Items: 56