VCX variable charge X-linked

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: VCX
Type: protein-coding
Description: variable charge X-linked
Entrez Gene ID: 26609
Genome: hg19
Position: chrX:7,810,303-7,812,184
Genome: hg38
Position: chrX:7,842,262-7,844,143
MIM: 300229 OMIM
HGNC: HGNC:12667 HGNC
Ensembl: ENSG00000182583 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	8
not provided	10	0
Uncertain significance	0	2

Ranking

	ClinVar
	0
	0
	0
	6
	4

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

Locus Zoom

Variants

Search Word

Target data	:	MGeND data only
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Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

Search Word

Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
Category	:
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Filtering	:

Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	VCX-10r
SYNONYM	VCX-B1
SYNONYM	VCX1
SYNONYM	VCX10R
SYNONYM	VCXB1
MIM	300229 OMIM
HGNC	HGNC:12667 HGNC
Ensembl	ENSG00000182583 Ensembl
AllianceGenome	HGNC:12667

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000381059.7	hg38	chrX	7,842,262	7,844,143	1,882
ENST00000620630.2	hg38	chrX	7,843,198	7,844,143	946
ENST00000688183.1	hg38	chrX	7,843,171	7,844,143	973
ENST00000692567.1	hg38	chrX	7,843,179	7,844,102	924
ENST00000341408.6	hg38	chrX	7,843,088	7,844,113	1,026
ENST00000381059.7	hg19	chrX	7,810,303	7,812,184	1,882
ENST00000341408.6	hg19	chrX	7,811,129	7,812,154	1,026
ENST00000688183.1	hg19	chrX	7,811,212	7,812,184	973
ENST00000692567.1	hg19	chrX	7,811,220	7,812,143	924
ENST00000620630.2	hg19	chrX	7,811,239	7,812,184	946

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