VCV002425382.4 - ClinVar

NC_000001.10:g.(?_61548464)_(67861772_?)del

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_000001.10:g.(?_61548464)_(67861772_?)del

Variation ID: 2425382 Accession: VCV002425382.4

Type and length

Deletion, 6,313,309 bp

Location

Cytogenetic: 1p31.3 1: 61548464-67861772 (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, 2023	Jun 9, 2024	Aug 20, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NC_000001.10:g.(?_61548464)_(67861772_?)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.
NFIA		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	307	346
AK4		-	-	GRCh38 GRCh37	15	41
ALG6		-	-	GRCh38 GRCh37	771	805
ANGPTL3		-	-	GRCh38 GRCh37	-	123
ATG4C		-	-	GRCh38 GRCh37	27	54
C1orf141	-	-	-	GRCh38 GRCh37	1	27
CACHD1		-	-	GRCh38 GRCh37	85	111
DNAI4		-	-	GRCh38 GRCh37	59	89
DNAJC6		-	-	GRCh38 GRCh37	312	343
DOCK7		-	-	GRCh38 GRCh37	1584	1732

There are 24 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)	criteria provided, single submitter	Aug 20, 2022	RCV003116397.5

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 (Aug 20, 2022)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	not provided Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV003794842.3 First in ClinVar: Feb 13, 2023 Last updated: Jun 09, 2024	Publications: PubMed (5) PubMed: 27081522‚ 31730271‚ 24098143‚ 31754721‚ 33288889 Comment: A gross deletion of the genomic region encompassing the full coding sequence of the NFIA gene has been identified. Loss-of-function variants in NFIA are known … (more) A gross deletion of the genomic region encompassing the full coding sequence of the NFIA gene has been identified. Loss-of-function variants in NFIA are known to be pathogenic (PMID: 27081522, 31730271). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. Isolated whole-gene deletions of NFIA have not been reported in the literature. However, larger copy number events that include this gene have been reported (PMID: 24098143, 31754721, 33288889). For these reasons, this variant has been classified as Pathogenic. (less)

Comment:

A gross deletion of the genomic region encompassing the full coding sequence of the NFIA gene has been identified. Loss-of-function variants in NFIA are known to be pathogenic (PMID: 27081522, 31730271). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes. Isolated whole-gene deletions of NFIA have not been reported in the literature. However, larger copy number events that include this gene have been reported (PMID: 24098143, 31754721, 33288889). For these reasons, this variant has been classified as Pathogenic.

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

Title	Author	Journal	Year	Link
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.	Tønne E	European journal of human genetics : EJHG	2021	PMID: 33288889
Molecular Diagnosis of Craniosynostosis Using Targeted Next-Generation Sequencing.	Yoon JG	Neurosurgery	2020	PMID: 31754721
Variants in nuclear factor I genes influence growth and development.	Zenker M	American journal of medical genetics. Part C, Seminars in medical genetics	2019	PMID: 31730271
Truncating mutation in NFIA causes brain malformation and urinary tract defects.	Negishi Y	Human genome variation	2015	PMID: 27081522
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.	Sajan SA	PLoS genetics	2013	PMID: 24098143

Text-mined citations for this variant ...

Record last updated Sep 30, 2024

ClinVar Genomic variation as it relates to human health

NC_000001.10:g.(?_61548464)_(67861772_?)del

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...