U.S. flag

An official website of the United States government

GRCh38/hg38 1p31.1(chr1:70716347-71407975)x3 AND See cases

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 18, 2014
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:
RCV000143773.5

Allele description [Variation Report for GRCh38/hg38 1p31.1(chr1:70716347-71407975)x3]

GRCh38/hg38 1p31.1(chr1:70716347-71407975)x3

Genes:
  • LOC129930762:ATAC-STARR-seq lymphoblastoid active region 1198 [Gene]
  • LOC129930761:ATAC-STARR-seq lymphoblastoid silent region 991 [Gene]
  • LOC129388549:MPRA-validated peak284 silencer [Gene]
  • ZRANB2-AS1:ZRANB2 antisense RNA 1 [Gene - HGNC]
  • ZRANB2-DT:ZRANB2 divergent transcript [Gene - HGNC]
  • LINC01788:long intergenic non-protein coding RNA 1788 [Gene - HGNC]
  • MIR186:microRNA 186 [Gene - HGNC]
  • NEGR1:neuronal growth regulator 1 [Gene - OMIM - HGNC]
  • PTGER3:prostaglandin E receptor 3 [Gene - OMIM - HGNC]
  • ZRANB2:zinc finger RANBP2-type containing 2 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
1p31.1
Genomic location:
Preferred name:
GRCh38/hg38 1p31.1(chr1:70716347-71407975)x3
HGVS:
  • NC_000001.11:g.(?_70716347)_(71407975_?)dup
  • NC_000001.10:g.(?_71182030)_(71873658_?)dup
Links:
dbVar: nssv3395479; dbVar: nsv996270
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
SCV000183700ISCA site 1

See additional submitters

no assertion criteria provided
Likely benign
(Mar 18, 2014) 		maternalclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedmaternalyes1not 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 1, SCV000183700.4

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

Last Updated: May 7, 2024