VCV000544685.1 - ClinVar

GRCh37/hg19 17p13.3(chr17:1-2538512)x4,5

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

no assertion criteria provided

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

GRCh37/hg19 17p13.3(chr17:1-2538512)x4,5

Variation ID: 544685 Accession: VCV000544685.1

Type and length

copy number gain, -

Location

Cytogenetic: 17p13.3 17: 1-2538512 (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	Jan 28, 2019	Jan 28, 2019	Apr 1, 2018

HGVS

Protein change

Other names

17p13.3(1-2538512)x4,5
17p13.3(525-2529405)x4,5

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.
PAFAH1B1		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	534	619
ABR		No evidence available	No evidence available	GRCh38 GRCh38 GRCh38 GRCh37	54	183
PITPNA		No evidence available	No evidence available	GRCh38 GRCh37	8	114
YWHAE		No evidence available	No evidence available	GRCh38 GRCh38 GRCh37	69	209
BHLHA9		-	-	GRCh38 GRCh37	60	187
CRK		-	-	GRCh38 GRCh38 GRCh37	15	130
DOC2B		-	-	GRCh38 GRCh38 GRCh37	26	79
DPH1		-	-	GRCh38 GRCh37	104	205
GEMIN4		-	-	GRCh38 GRCh37	186	294
GLOD4	-	-	-	GRCh38 GRCh37	21	132

There are 33 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.
Bilateral fetal pyelectasis Echogenic fetal bowel Neurodevelopmental abnormality Partial agenesis of the corpus callosum Ventriculomegaly	Uncertain significance (1)	no assertion criteria provided	Apr 1, 2018	RCV000754117.1

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.
Uncertain significance (Apr 01, 2018)	no assertion criteria provided Method: clinical testing	Partial agenesis of the corpus callosum Ventriculomegaly Echogenic fetal bowel Bilateral fetal pyelectasis Neurodevelopmental abnormality Affected status: yes Allele origin: unknown	Department of Obstetrics and Gynecology, Montefiore Medical Center Accession: SCV000747897.1 First in ClinVar: Jan 28, 2019 Last updated: Jan 28, 2019	Publications: PubMed (1) PubMed: 29858378 Comment: Quadruplication of unknown significance, not previously reported at the site of a known duplication site; new pathogenic variant vs dose dependent phenotype. Number of individuals with the variant: 1 Secondary finding: no

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
17p13.3 quadruplication: a prenatal and postpartum clinical characterization of a copy number variant.	Farris N	Cold Spring Harbor molecular case studies	2018	PMID: 29858378

Text-mined citations for this variant ...

Record last updated Oct 15, 2023

ClinVar Genomic variation as it relates to human health

GRCh37/hg19 17p13.3(chr17:1-2538512)x4,5

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...