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GRCh38/hg38 7q36.3(chr7:155807064-155807664)x3 AND See cases

Germline classification:
conflicting data from submitters (1 submission)
Last evaluated:
Feb 4, 2013
Review status:
(0/4) 0 stars out of maximum of 4 stars
conflicting data from submitters (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:
RCV000136706.4

Allele description

GRCh38/hg38 7q36.3(chr7:155807064-155807664)x3

Gene:
SHH:sonic hedgehog signaling molecule [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
7q36.3
Genomic location:
Preferred name:
GRCh38/hg38 7q36.3(chr7:155807064-155807664)x3
HGVS:
  • NC_000007.14:g.(?_155807064)_(155807664_?)dup
  • NC_000007.12:g.(?_155292519)_(155293119_?)dup
  • NC_000007.13:g.(?_155599758)_(155600358_?)dup
Links:
dbVar: nssv3395528; dbVar: nssv3397463; dbVar: nssv581524; dbVar: nssv582111; dbVar: nsv534049
Observations:
4

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
SCV000176821ISCA site 2

See additional submitters

no assertion criteria provided
conflicting data from submitters
(Feb 4, 2013) 		de novo, not providedclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot providedyes3not providednot providednot providednot providedclinical testing
not providedde novoyes1not 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 2, SCV000176821.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)
2not provided1not providednot providedclinical testing PubMed (1)
3not provided1not providednot providedclinical testing PubMed (1)
4not provided1not providednot providedclinical testing PubMed (1)

Description

Uncertain significance(1), Benign (3)

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1de novoyesnot providednot providedDiscovery1not providednot providednot provided
2not providedyesnot providednot providedDiscovery1not providednot providednot provided
3not providedyesnot providednot providedDiscovery1not providednot providednot provided
4not providedyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: Apr 23, 2022