Related gene-specific medical variations for Gene (Select 85445) - ClinVar - NCBI

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Links from Gene

Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063474	GRCh37/hg19 16q23.1(chr16:76339977-76411476)x1	CNTNAP4	Copy number loss	not specified	GUncertain significance
Select item 2685576	GRCh37/hg19 16q23.1(chr16:76291621-76722658)x1	CNTNAP4	Copy number loss	not provided	GUncertain significance
Select item 2684817	GRCh37/hg19 16q23.1(chr16:75989007-76546270)x3	CNTNAP4	Copy number gain	not provided	GUncertain significance
Select item 1807969	GRCh37/hg19 16q23.1(chr16:76575950-76638633)x1	CNTNAP4	Copy number loss	not provided	GUncertain significance
Select item 1526522	GRCh37/hg19 16q23.1(chr16:76000179-76371082)	CNTNAP4	Copy number gain	not specified	GUncertain significance
Select item 1340035	GRCh37/hg19 16q23.1(chr16:76457786-76610695)x1	CNTNAP4	Copy number loss	not provided	GUncertain significance
Select item 815836	GRCh37/hg19 16q23.1(chr16:76324005-76656042)x1	CNTNAP4	Copy number loss	not provided	GUncertain significance
Select item 815835	GRCh37/hg19 16q23.1(chr16:76070955-77090139)x3	CNTNAP4	Copy number gain	not provided	GUncertain significance
Select item 815834	GRCh37/hg19 16q23.1(chr16:75822770-77037952)x3	CNTNAP4	Copy number gain	not provided	GUncertain significance
Select item 686075	GRCh37/hg19 16q23.1(chr16:76348941-76374538)x1	CNTNAP4	Copy number loss	not provided	GUncertain significance
Select item 685507	GRCh37/hg19 16q23.1(chr16:76009327-76656042)x1	CNTNAP4	Copy number loss	not provided	GUncertain significance
Select item 564346	GRCh37/hg19 16q23.1(chr16:75929490-76742027)x3	CNTNAP4	Copy number gain	not provided	GLikely benign
Select item 564345	GRCh37/hg19 16q23.1(chr16:75799117-77172017)x3	CNTNAP4	Copy number gain	not provided	GUncertain significance