VCV002663780.1 - ClinVar

NC_000023.11:g.(?_66445907)_(78172208_?)dup

Germline

Classification

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

(1)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Pathogenic

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NC_000023.11:g.(?_66445907)_(78172208_?)dup

Variation ID: 2663780 Accession: VCV002663780.1

Type and length

Duplication, 11,726,302 bp

Location

Cytogenetic: Xq12-21.1 X: 66445907-78172208 (GRCh38) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Mar 11, 2024	Mar 10, 2024	Jul 1, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NC_000023.11:g.(?_66445907)_(78172208_?)dup

Protein change

Other names

Canonical SPDI

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
EFNB1		Sufficient evidence for dosage pathogenicity	Little evidence for dosage pathogenicity	GRCh38 GRCh37	154	289
AR		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	822	1038
ATP7A		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	1967	2159
ATRX		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	2330	2493
DLG3		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	189	341
EDA		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	591	732
HDAC8		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	322	457
MAGT1		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	218	414
NEXMIF		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	1033	1172
NONO		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	149	282

There are 198 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38).

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Xq13q21 duplication	Pathogenic (1)	criteria provided, single submitter	Jul 1, 2023	RCV003885331.1

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Pathogenic (Jul 01, 2023)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: research	Xq13q21 duplication Affected status: yes Allele origin: maternal	DECIPHERD-UDD, Universidad del Desarrollo Accession: SCV004170998.1 First in ClinVar: Mar 10, 2024 Last updated: Mar 10, 2024	Publications: PubMed (1) PubMed: 38177409 Clinical Features: Small for gestational age (present) , Birth length less than 3rd percentile (present) , Severe failure to thrive (present) , Short stature (present) , Proportionate … (more) Small for gestational age (present) , Birth length less than 3rd percentile (present) , Severe failure to thrive (present) , Short stature (present) , Proportionate short stature (present) , Global developmental delay (present) , Microtia (present) , Micrognathia (present) , Long philtrum (present) , Downslanted palpebral fissures (present) , Broad forehead (present) , Anteverted nares (present) , Full cheeks (present) , High palate (present) , Downturned corners of mouth (present) , Thin upper lip vermilion (present) , Thoracic aortic aneurysm (present) , Bicuspid aortic valve (present) , Aortic root aneurysm (present) , Congenital laryngomalacia (present) , Micropenis (present) , Lower limb asymmetry (present) , Atopic eczema (present) (less)

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for germline classification of this variant

Title	Author	Journal	Year	Link
Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile.	Poli MC	European journal of human genetics : EJHG	2024	PMID: 38177409

Text-mined citations for this variant ...

Record last updated Sep 01, 2024

ClinVar Genomic variation as it relates to human health

NC_000023.11:g.(?_66445907)_(78172208_?)dup

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...