GRCh37/hg19 19p13.2(chr19:7184327-7184648)x1 AND not provided

Clinical significance:Uncertain significance (Last evaluated: Apr 1, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000997021.2

Allele description [Variation Report for GRCh37/hg19 19p13.2(chr19:7184327-7184648)x1]

GRCh37/hg19 19p13.2(chr19:7184327-7184648)x1

Gene:
INSR:insulin receptor [Gene - OMIM - HGNC]
Variant type:
copy number loss
Cytogenetic location:
19p13.2
Genomic location:
Chr19: 7184327 - 7184648 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 19p13.2(chr19:7184327-7184648)x1
HGVS:
NC_000019.9:g.(?_7184327)_(7184648_?)del
Observations:
1

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001152079CeGaT Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Uncertain significance
(Apr 1, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Praxis fuer Humangenetik Tuebingen, SCV001152079.7

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

Last Updated: Nov 20, 2021

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