VCV000058548.2 - ClinVar

GRCh38/hg38 10q11.22-11.23(chr10:45999930-49937908)x1

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.

Uncertain significance

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

GRCh38/hg38 10q11.22-11.23(chr10:45999930-49937908)x1

Variation ID: 58548 Accession: VCV000058548.2

Type and length

copy number loss, 4,827,713 bp

Location

Cytogenetic: 10q11.22-11.23 10: 45999930-49937908 (GRCh38) [ NCBI UCSC ] 10: 49390075-52518989 (GRCh37) [ NCBI UCSC ] 10: 49060081-52188995 (NCBI36) [ 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	Apr 17, 2019	Apr 17, 2019	Mar 26, 2019

HGVS

Nucleotide	Protein	Molecular consequence
NC_000010.11:g.(?_45999930)_(49937908_?)del
NC_000010.10:g.(?_49390075)_(52518989_?)del
NC_000010.9:g.(?_49060081)_(52188995_?)del

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

dbVar: nssv579670 dbVar: nsv531028 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.
GDF2		No evidence available	No evidence available	GRCh38 GRCh37	264	381
AGAP9	-	-	-	GRCh38 GRCh37	-	111
ANTXRL	-	-	-	GRCh38	-	55
ANXA8		-	-	GRCh38 GRCh38 GRCh37	-	123
ANXA8L1	-	-	-	GRCh38 GRCh37	10	120
ARHGAP22		-	-	GRCh38 GRCh37	74	162
ARHGAP22-IT1	-	-	-	GRCh38	-	22
C10orf53	-	-	-	GRCh38 GRCh37	2	88
C10orf71	-	-	-	GRCh38 GRCh37	22	109
C10orf71-AS1	-	-	-	GRCh38	-	23

There are 104 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.

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.
See cases	Uncertain significance (1)	criteria provided, single submitter	Mar 26, 2019	RCV000052317.6

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.
Uncertain significance (Mar 26, 2019)	criteria provided, single submitter (Kaminsky et al. (Genet Med. 2011)) Method: clinical testing	See cases Affected status: yes Allele origin: de novo	GeneDx Accession: SCV000079669.5 First in ClinVar: Aug 03, 2013 Last updated: Apr 17, 2019	Comment: The deleted interval contains 27 genes and transcripts; three of these genes, ERCC6, CHAT, and SLC18A3 are associated with inherited human disorders. Recurrent deletions of … (more) The deleted interval contains 27 genes and transcripts; three of these genes, ERCC6, CHAT, and SLC18A3 are associated with inherited human disorders. Recurrent deletions of 10q11.22 have been described in individuals with a highly variable phenotype including developmental delay and intellectual disability. Autism spectrum disorders, epilepsy, and dysmorphic features have also been reported. Parental testing showed that deletions of this region were inherited from apparently normal parents in most cases, suggesting that additional factors likely play a role in the development of an abnormal phenotype. As such, the clinical consequence of this deletion is unknown. This region in its entirety is not known to vary in copy number in the normal population. (less) Number of individuals with the variant: 1 Clinical Features: Intrauterine growth retardation (present) Method: Microarray

Comment:

The deleted interval contains 27 genes and transcripts; three of these genes, ERCC6, CHAT, and SLC18A3 are associated with inherited human disorders. Recurrent deletions of 10q11.22 have been described in individuals with a highly variable phenotype including developmental delay and intellectual disability. Autism spectrum disorders, epilepsy, and dysmorphic features have also been reported. Parental testing showed that deletions of this region were inherited from apparently normal parents in most cases, suggesting that additional factors likely play a role in the development of an abnormal phenotype. As such, the clinical consequence of this deletion is unknown. This region in its entirety is not known to vary in copy number in the normal population.

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.

Comment:

Citations for germline classification of this variant

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for this variant ...

Record last updated Oct 15, 2023

ClinVar Genomic variation as it relates to human health

GRCh38/hg38 10q11.22-11.23(chr10:45999930-49937908)x1

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...