GRCh37/hg19 7q11.21(chr7:62495083-64927758)x1 AND See cases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 18, 2018
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:: RCV001263023.1

Allele description [Variation Report for GRCh37/hg19 7q11.21(chr7:62495083-64927758)x1]

GRCh37/hg19 7q11.21(chr7:62495083-64927758)x1

Genes:

ERV3-1:endogenous retrovirus group 3 member 1, envelope [Gene - OMIM - HGNC]
ZNF107:zinc finger protein 107 [Gene - OMIM - HGNC]
ZNF117:zinc finger protein 117 [Gene - OMIM - HGNC]
ZNF138:zinc finger protein 138 [Gene - OMIM - HGNC]
ZNF273:zinc finger protein 273 [Gene - OMIM - HGNC]
ZNF679:zinc finger protein 679 [Gene - HGNC]
ZNF680:zinc finger protein 680 [Gene - HGNC]
ZNF727:zinc finger protein 727 [Gene - HGNC]
ZNF735:zinc finger protein 735 [Gene - HGNC]
ZNF736:zinc finger protein 736 [Gene - HGNC]
ZNF92:zinc finger protein 92 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

7q11.21

Genomic location:

Chr7: 62495083 - 64927758 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 7q11.21(chr7:62495083-64927758)x1

HGVS:

NC_000007.13:g.(62495083_?)_(?_64927758)del

Condition(s)

Name:: See cases [See the Variation display for details]
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001441098	HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology - CSER-SouthSeq	no assertion criteria provided	Uncertain significance (Jul 18, 2018)	unknown	research

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001441098

HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology - CSER-SouthSeq

no assertion criteria provided

Uncertain significance
(Jul 18, 2018)

unknown

research

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	1	not provided	not provided	1	not provided	research

Details of each submission

From HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology - CSER-SouthSeq, SCV001441098.1

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

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

Last Updated: Mar 26, 2023

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