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GRCh37/hg19 1p34.2(chr1:40962859-41375802)x1 AND See cases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 16, 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:
RCV000511219.3

Allele description [Variation Report for GRCh37/hg19 1p34.2(chr1:40962859-41375802)x1]

GRCh37/hg19 1p34.2(chr1:40962859-41375802)x1

Genes:
  • CITED4:Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4 [Gene - OMIM - HGNC]
  • EXO5:exonuclease 5 [Gene - OMIM - HGNC]
  • MIR30C1:microRNA 30c-1 [Gene - OMIM - HGNC]
  • NFYC:nuclear transcription factor Y subunit gamma [Gene - OMIM - HGNC]
  • KCNQ4:potassium voltage-gated channel subfamily Q member 4 [Gene - OMIM - HGNC]
  • RIMS3:regulating synaptic membrane exocytosis 3 [Gene - OMIM - HGNC]
  • ZNF684:zinc finger protein 684 [Gene - HGNC]
Variant type:
copy number loss
Cytogenetic location:
1p34.2
Genomic location:
Chr1: 40962859 - 41375802 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 1p34.2(chr1:40962859-41375802)x1
HGVS:
NC_000001.10:g.(?_40962859)_(41375802_?)del
Links:
dbVar: nssv13642966; dbVar: nsv2773544
Observations:
1

Condition(s)

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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000585169ISCA site 1

See additional submitters

no assertion criteria provided
Uncertain significance
(Jun 16, 2014) 		paternalclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedpaternalyes1not 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, SCV000585169.1

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

Last Updated: May 7, 2024