GRCh37/hg19 Xq28(chrX:152372767-155233731) Detail (hg19) (ABCD1, ARHGAP4, ATP2B3, ATP6AP1, AVPR2, BGN, CLIC2, CTAG1B, TEX28, DKC1, DNASE1L1, DUSP9, EMD, F8, FLNA, G6PD, OPN1MW, GDI1, HCFC1, IDH3G, IRAK1, L1CAM, MAGEA1, MECP2, MPP1, MTCP1, PLXNB3, OPN1LW, RENBP, RPL10, SLC6A8, SSR4, TAFAZZIN, VBP1, NAA10, F8A1, UBL4A, TMEM187, LAGE3, SLC10A3, TKTL1, IKBKG, FAM50A, BCAP31, ZNF275, TREX2, SRPK3, CTAG2, TMLHE, PLXNA3, HAUS7, PDZD4, FAM3A, FUNDC2, BRCC3, H2AB3, CCNQ, RAB39B, GAB3, PNCK, ZFP92, CTAG1A, H2AB2, H2AB1, F8A2, F8A3, PNMA6E, OPN1MW2, SMIM9, CMC4)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
Genome browser

Information

Genome

Assembly	Position
hg19	chrX:152,372,767-155,233,731
hg38	chrX:153,106,941-156,004,066

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

ClinVar

Clinical Significance	Pathogenic
Review star
Show details

Links

Type	Database	ID	Link
Gene	MIM
	HGNC
	Ensembl
	NCBI
	Gene Cards
	OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic		no assertion criteria provided	syndromic X-linked intellectual disability Lubs type	unknown	Detail
Pathogenic		no assertion criteria provided	Chromosome Xq28 duplication syndrome	unknown	Detail

CIViC

[No Data.]

DisGeNET

[No Data.]

Annotation

Annotations

Descrption	Source	Links
GRCh37/hg19 Xq28(chrX:152372767-155233731) AND Syndromic X-linked intellectual disability Lubs type	ClinVar	Detail
GRCh37/hg19 Xq28(chrX:152372767-155233731) AND Chromosome Xq28 duplication syndrome	ClinVar	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
Genome: hg19
Position: chrX:152,372,767-155,233,731
Variant Type: cnv

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