U.S. flag

An official website of the United States government

GRCh38/hg38 7q35(chr7:143735739-144254897)x3 AND See cases

Germline classification:
Benign (1 submission)
Last evaluated:
Jan 30, 2010
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:
RCV000133872.5

Allele description [Variation Report for GRCh38/hg38 7q35(chr7:143735739-144254897)x3]

GRCh38/hg38 7q35(chr7:143735739-144254897)x3

Genes:
  • ARHGEF35-AS1:ARHGEF35 antisense RNA 1 [Gene - HGNC]
  • LOC129999522:ATAC-STARR-seq lymphoblastoid active region 26794 [Gene]
  • LOC129999523:ATAC-STARR-seq lymphoblastoid active region 26795 [Gene]
  • LOC129999520:ATAC-STARR-seq lymphoblastoid silent region 18726 [Gene]
  • LOC129999521:ATAC-STARR-seq lymphoblastoid silent region 18727 [Gene]
  • LOC129999524:ATAC-STARR-seq lymphoblastoid silent region 18728 [Gene]
  • CTAGE4:CTAGE family member 4 [Gene - OMIM - HGNC]
  • CTAGE6:CTAGE family member 6 [Gene - HGNC]
  • LOC129389908:MPRA-validated peak6808 silencer [Gene]
  • LOC129389909:MPRA-validated peak6810 silencer [Gene]
  • OR2A1-AS1:OR2A1 antisense RNA 1 [Gene - HGNC]
  • ARHGEF35:Rho guanine nucleotide exchange factor 35 [Gene - HGNC]
  • TCAF1:TRPM8 channel associated factor 1 [Gene - OMIM - HGNC]
  • OR2A12:olfactory receptor family 2 subfamily A member 12 [Gene - HGNC]
  • OR2A14:olfactory receptor family 2 subfamily A member 14 [Gene - HGNC]
  • OR2A25:olfactory receptor family 2 subfamily A member 25 [Gene - HGNC]
  • OR2A2:olfactory receptor family 2 subfamily A member 2 [Gene - HGNC]
  • OR2A42:olfactory receptor family 2 subfamily A member 42 [Gene - HGNC]
  • OR2A5:olfactory receptor family 2 subfamily A member 5 [Gene - HGNC]
  • OR2F1:olfactory receptor family 2 subfamily F member 1 [Gene - OMIM - HGNC]
  • OR2F2:olfactory receptor family 2 subfamily F member 2 [Gene - HGNC]
  • OR6B1:olfactory receptor family 6 subfamily B member 1 [Gene - HGNC]
Variant type:
copy number gain
Cytogenetic location:
7q35
Genomic location:
Preferred name:
GRCh38/hg38 7q35(chr7:143735739-144254897)x3
HGVS:
  • NC_000007.14:g.(?_143735739)_(144254897_?)dup
  • NC_000007.12:g.(?_143063765)_(143582923_?)dup
  • NC_000007.13:g.(?_143432832)_(143951990_?)dup
Links:
dbVar: nssv575786; dbVar: nsv491957
Observations:
1

Condition(s)

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

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000173289ISCA site 4

See additional submitters

no assertion criteria provided
Benign
(Jan 30, 2010) 		unknownclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot providedyes1not providednot providednot providednot providedclinical testing

Citations

PubMed

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, et al.

Am J Hum Genet. 2010 May 14;86(5):749-64. doi: 10.1016/j.ajhg.2010.04.006. Review.

PubMed [citation]
PMID:
20466091
PMCID:
PMC2869000

Details of each submission

From ISCA site 4, SCV000173289.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: May 7, 2024