Related gene-specific medical variations for Gene (Select 253559) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807683	GRCh37/hg19 3p12.2-12.1(chr3:82896300-85764904)x3	CADM2	Copy number gain	not provided	GUncertain significance
Select item 980021	GRCh37/hg19 3p12.1(chr3:84958561-85175858)x3	CADM2	Copy number gain	not provided	GLikely benign
Select item 980020	GRCh37/hg19 3p12.1(chr3:85323182-85578035)x1	CADM2	Copy number loss	not provided	GLikely benign
Select item 814461	GRCh37/hg19 3p12.1(chr3:84951675-85119041)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 814460	GRCh37/hg19 3p12.1(chr3:83681388-85570265)x3	CADM2	Copy number gain	not provided	GUncertain significance
Select item 688918	GRCh37/hg19 3p12.1(chr3:85462795-85678555)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 688880	GRCh37/hg19 3p12.1(chr3:84757732-85375831)x3	CADM2	Copy number gain	not provided	GUncertain significance
Select item 688595	GRCh37/hg19 3p12.1(chr3:85534492-85630237)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 687336	GRCh37/hg19 3p12.1(chr3:85545466-85630145)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 687296	GRCh37/hg19 3p12.1(chr3:85534558-85630237)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 687282	GRCh37/hg19 3p12.1(chr3:85555420-85622910)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 685501	GRCh37/hg19 3p12.1(chr3:85988337-86080939)x3	CADM2	Copy number gain	not provided	GUncertain significance
Select item 562792	GRCh37/hg19 3p12.1(chr3:85947973-86315425)x1	CADM2	Copy number loss	not provided	GUncertain significance
Select item 562791	GRCh37/hg19 3p12.1(chr3:85304378-85474415)x1	CADM2	Copy number loss	not provided	GLikely benign
Select item 562790	GRCh37/hg19 3p12.2-12.1(chr3:82906524-85764904)x3	CADM2	Copy number gain	not provided	GUncertain significance
Select item 393805	GRCh37/hg19 3p12.1(chr3:85119132-85362677)x1	CADM2	Copy number loss	See cases	GLikely benign
Select item 226159	GRCh37/hg19 3p12.1(chr3:85561190-85612793)	CADM2	Copy number loss	Abnormal esophagus morphology	GBenign
Select item 221698	GRCh38/hg38 3p12.1(chr3:85427867-85558987)x1	CADM2	Copy number loss	Premature ovarian failure	GBenign
Select item 151884	GRCh38/hg38 3p12.1(chr3:85521116-85566418)x1	CADM2	Copy number loss	See cases	GBenign
Select item 144855	GRCh38/hg38 3p12.1(chr3:85408307-85566418)x1	CADM2	Copy number loss	See cases	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 20