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GRCh38/hg38 1p31.3(chr1:65473801-65541817)x3 AND See cases

Germline classification:
Benign (1 submission)
Last evaluated:
Apr 30, 2011
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:
RCV000140154.3

Allele description [Variation Report for GRCh38/hg38 1p31.3(chr1:65473801-65541817)x3]

GRCh38/hg38 1p31.3(chr1:65473801-65541817)x3

Gene:
LEPR:leptin receptor [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
1p31.3
Genomic location:
Preferred name:
GRCh38/hg38 1p31.3(chr1:65473801-65541817)x3
HGVS:
  • NC_000001.11:g.(?_65473801)_(65541817_?)dup
  • NC_000001.10:g.(?_65939484)_(66007500_?)dup
Links:
dbVar: nssv1609236; dbVar: nsv931327
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
SCV000180826GeneDx
no assertion criteria provided
Benign
(Apr 30, 2011) 		not providedclinical testing

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000180826.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not providedyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: Apr 23, 2022