VCV001341055.1 - ClinVar

GRCh37/hg19 13q21.1-31.2(chr13:59574760-89410027)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.

Pathogenic

no assertion criteria provided

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

GRCh37/hg19 13q21.1-31.2(chr13:59574760-89410027)x1

Variation ID: 1341055 Accession: VCV001341055.1

Type and length

copy number loss, 29,835,268 bp

Location

Cytogenetic: 13q21.1-31.2 13: 59574760-89410027 (GRCh37) [ 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	Feb 13, 2022	Feb 13, 2022	Feb 1, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NC_000013.10:g.(?_59574760)_(89410027_?)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

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.
EDNRB		Little evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	92	384
PCDH9		No evidence available	No evidence available	GRCh38 GRCh37	63	151
ACOD1		-	-	GRCh38 GRCh37	5	75
ATXN8OS		-	-	GRCh38 GRCh37	11	108
BORA		-	-	GRCh38 GRCh37	29	103
CLN5		-	-	GRCh38 GRCh37	598	798
COMMD6		-	-	GRCh38 GRCh37	2	70
DACH1		-	-	GRCh38 GRCh37	39	104
DIAPH3		-	-	GRCh38 GRCh37	404	507
DIS3		-	-	GRCh38 GRCh37	61	141

There are 27 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) 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.
not provided	Pathogenic (1)	no assertion criteria provided	Feb 1, 2021	RCV001834426.1

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 (Feb 01, 2021)	no assertion criteria provided Method: clinical testing	not provided Affected status: unknown Allele origin: germline	Quest Diagnostics Nichols Institute San Juan Capistrano Accession: SCV002095631.1 First in ClinVar: Feb 13, 2022 Last updated: Feb 13, 2022	Comment: The copy number loss of 13q21.1q31.2 involves numerous protein-coding genes and is expected to cause phenotypic and/or developmental abnormalities. Deletions of 13q have been reported … (more) The copy number loss of 13q21.1q31.2 involves numerous protein-coding genes and is expected to cause phenotypic and/or developmental abnormalities. Deletions of 13q have been reported in patients with multiple clinical phenotypes, which include a wide phenotypic spectrum varying with respect to the location and size of the deletion region (Quelin, et al. Eur J Med Genet. 2009;52:41-46, PMID: 19022413; Cordova-Fletes et al., Clin Dysmorphol. 2017 Jan;26(1):33-37. PMID: 27750267; Chatmethakul et al., J Pediatr Genet. 2019 Sep;8(3):142-146. PMID: 31406620). The main clinical features are developmental delay, intellectual disability, craniofacial dysmorphism and various congenital defects. Brain malformation, bilateral hearing loss, heterochromia iridis and hypopigmentation are also reported. Deletion of the EDNRB gene may be involved in variable manifestations of Waardenburg syndrome type 4A (OMIM 277580) observed in those patients carrying 13q deletions. Loss of SPRY2 gene has been implicated in lens cell proliferation and differentiation for the congenital cataract phenotype. This large deletion also includes other genes associated with OMIM phenotypes: ATXN8 (OMIM 608768), DIAPH3 (OMIM 609129), ATXN8OS (OMIM 608768), SLITRK1 (OMIM 137580), PIBF1 (OMIM 617767), CLN5 (OMIM 256731), FBXL3 (OMIM 606220), SLITRK6 (OMIM 221200). (less)

Comment:

The copy number loss of 13q21.1q31.2 involves numerous protein-coding genes and is expected to cause phenotypic and/or developmental abnormalities. Deletions of 13q have been reported in patients with multiple clinical phenotypes, which include a wide phenotypic spectrum varying with respect to the location and size of the deletion region (Quelin, et al. Eur J Med Genet. 2009;52:41-46, PMID: 19022413; Cordova-Fletes et al., Clin Dysmorphol. 2017 Jan;26(1):33-37. PMID: 27750267; Chatmethakul et al., J Pediatr Genet. 2019 Sep;8(3):142-146. PMID: 31406620). The main clinical features are developmental delay, intellectual disability, craniofacial dysmorphism and various congenital defects. Brain malformation, bilateral hearing loss, heterochromia iridis and hypopigmentation are also reported. Deletion of the EDNRB gene may be involved in variable manifestations of Waardenburg syndrome type 4A (OMIM 277580) observed in those patients carrying 13q deletions. Loss of SPRY2 gene has been implicated in lens cell proliferation and differentiation for the congenital cataract phenotype. This large deletion also includes other genes associated with OMIM phenotypes: ATXN8 (OMIM 608768), DIAPH3 (OMIM 609129), ATXN8OS (OMIM 608768), SLITRK1 (OMIM 137580), PIBF1 (OMIM 617767), CLN5 (OMIM 256731), FBXL3 (OMIM 606220), SLITRK6 (OMIM 221200).

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 Sep 01, 2024

ClinVar Genomic variation as it relates to human health

GRCh37/hg19 13q21.1-31.2(chr13:59574760-89410027)x1

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...