GRCh38/hg38 Xp22.33(chrX:2444467-2970550)x3 AND See cases

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Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 12, 2011
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000052291.6

Allele description

GRCh38/hg38 Xp22.33(chrX:2444467-2970550)x3

Genes:

ARSD-AS1:ARSD antisense RNA 1 [Gene - HGNC]
CD99:CD99 molecule (Xg blood group) [Gene - OMIM - OMIM - HGNC]
XG:Xg blood group [Gene - OMIM - HGNC]
ARSD:arylsulfatase D [Gene - OMIM - HGNC]
ARSE:arylsulfatase E (chondrodysplasia punctata 1) [Gene - OMIM - HGNC]
DHRSX:dehydrogenase/reductase X-linked [Gene - HGNC]
GYG2:glycogenin 2 [Gene - OMIM - HGNC]
LINC00102:long intergenic non-protein coding RNA 102 [Gene - HGNC]
MIR6089:microRNA 6089 [Gene - HGNC]
ZBED1:zinc finger BED-type containing 1 [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

Xp22.33

Genomic location:

Preferred name:

GRCh38/hg38 Xp22.33(chrX:2444467-2970550)x3

HGVS:

NC_000023.11:g.(?_2444467)_(2970550_?)dup
NC_000023.10:g.(?_2362508)_(2888591_?)dup
NC_000023.9:g.(?_2372508)_(2898591_?)dup

Links:

dbVar: nssv581395; dbVar: nsv531002

Observations:

Condition(s)

Name:: See cases [See the Variation display for details]
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000079642	ISCA site 1 See additional submitters International Standards For Cytogenomic Arrays Consortium (ISCA)	criteria provided, single submitter (Submitter's publication)	Uncertain significance (Aug 12, 2011)	maternal	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000079642

ISCA site 1

See additional submitters

criteria provided, single submitter

(Submitter's publication)

Uncertain significance
(Aug 12, 2011)

maternal

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	maternal	yes	1	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, et al.

Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9.

PubMed [citation]

PMID:: 21844811
PMCID:: PMC3661946

Details of each submission

From ISCA site 1, SCV000079642.6

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	maternal	yes	not provided	not provided	Discovery		1	not provided	not provided	not provided

Last Updated: Jul 15, 2017

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