Related gene-specific medical variations for Gene (Select 1740) - ClinVar

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Links from Gene

Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063216	GRCh37/hg19 11q14.1(chr11:83920298-84049580)x1	DLG2	Copy number loss	not specified	GUncertain significance
Select item 2688941	NM_001142699.3(DLG2):c.335G>A (p.Trp112Ter)	DLG2 (W112*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2688940	NM_001142699.3(DLG2):c.770G>A (p.Arg257Gln)	DLG2, LOC126861281 (R101Q +8 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2685414	GRCh37/hg19 11q14.1(chr11:84331762-84637693)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 2685413	GRCh37/hg19 11q14.1(chr11:83853998-84135406)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 2685412	GRCh37/hg19 11q14.1(chr11:83827867-84146142)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 2296406	NM_001142699.3(DLG2):c.800C>T (p.Ser267Phe)	DLG2, LOC126861281 (S279F +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1340393	GRCh37/hg19 11q14.1(chr11:84070025-84430577)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 1340076	GRCh37/hg19 11q14.1(chr11:84068267-84316748)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 1219849	NC_000011.10:g.85628257G>A	DLG2, LOC130006547 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 980961	GRCh37/hg19 11q14.1(chr11:84413218-84622563)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 980958	GRCh37/hg19 11q14.1(chr11:84977926-85065507)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 815448	GRCh37/hg19 11q14.1(chr11:84532769-84667581)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 815447	GRCh37/hg19 11q14.1(chr11:84511722-84654573)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 815446	GRCh37/hg19 11q14.1(chr11:84459458-84654573)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 688771	GRCh37/hg19 11q14.1(chr11:84310436-84437544)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 688480	GRCh37/hg19 11q14.1(chr11:84233859-84337708)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 688078	GRCh37/hg19 11q14.1(chr11:84068533-84315237)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 687909	GRCh37/hg19 11q14.1(chr11:84337707-84560640)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 685857	GRCh37/hg19 11q14.1(chr11:84688061-84858221)x3	DLG2	Copy number gain	not provided	GUncertain significance
Select item 685496	GRCh37/hg19 11q14.1(chr11:84386275-84666945)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 685317	GRCh37/hg19 11q14.1(chr11:84415752-84622563)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 685037	GRCh37/hg19 11q14.1(chr11:83325218-83432435)x1	DLG2	Copy number loss	not provided	GUncertain significance
Select item 684192	NM_018480.4(TMEM126B):c.-272T>A	DLG2, LOC130006547 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 671602	NM_018480.4(TMEM126B):c.-308C>T	DLG2, LOC130006547 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 563840	GRCh37/hg19 11q14.1(chr11:84171800-84479887)x3	DLG2	Copy number gain	not provided	GUncertain significance
Select item 545152	NC_000011.10:g.(?_84877230)_(84963429_?)del	DLG2	Deletion	Schizophrenia	GLikely pathogenic
Select item 545151	NC_000011.10:g.(?_84809995)_(84986152_?)del	DLG2	Deletion	Schizophrenia	GLikely pathogenic
Select item 442035	GRCh37/hg19 11q14.1(chr11:84005323-84315291)x1	DLG2	Copy number loss	See cases	GUncertain significance
Select item 395392	GRCh37/hg19 11q14.1(chr11:84157984-84367238)x1	DLG2	Copy number loss	See cases	GLikely benign
Select item 394449	GRCh37/hg19 11q14.1(chr11:84333985-84419443)x1	DLG2	Copy number loss	See cases	GBenign
Select item 394227	GRCh37/hg19 11q14.1(chr11:84214703-84477029)x1	DLG2	Copy number loss	See cases	GLikely benign
Select item 394101	GRCh37/hg19 11q14.1(chr11:84419443-84583725)x1	DLG2	Copy number loss	See cases	GBenign
Select item 150875	GRCh38/hg38 11q14.1(chr11:84446955-84708445)x1	DLG2	Copy number loss	See cases	GLikely benign

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Links from Gene

Items: 34