GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3 AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 4, 2019
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001258447.1

Allele description [Variation Report for GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3]

GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3

Genes:

AKNAD1:AKNA domain containing 1 [Gene - HGNC]
EEIG2:EEIG family member 2 [Gene - HGNC]
GPSM2:G protein signaling modulator 2 [Gene - OMIM - HGNC]
HENMT1:HEN methyltransferase 1 [Gene - OMIM - HGNC]
NBPF4:NBPF member 4 [Gene - OMIM - HGNC]
NBPF6:NBPF member 6 [Gene - OMIM - HGNC]
FNDC7:fibronectin type III domain containing 7 [Gene - HGNC]
PRPF38B:pre-mRNA processing factor 38B [Gene - HGNC]
STXBP3:syntaxin binding protein 3 [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

1p13.3

Genomic location:

Chr1: 108769288 - 109425488 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3

HGVS:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001435416	Quest Diagnostics Nichols Institute San Juan Capistrano	no assertion criteria provided	Uncertain significance (Oct 4, 2019)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001435416

Quest Diagnostics Nichols Institute San Juan Capistrano

no assertion criteria provided

Uncertain significance
(Oct 4, 2019)

germline

clinical testing

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV001435416.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Mar 26, 2023

ClinVar

Relating variation to medicine

GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3 AND not provided

Allele description [Variation Report for GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3]

GRCh37/hg19 1p13.3(chr1:108769288-109425488)x3

Condition(s)

Recent activity

Assertion and evidence details

Summary from all submissions

Details of each submission

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV001435416.1