GRCh37/hg19 7q21.2(chr7:92317752-92449293)x3 AND not provided

Clinical significance:Benign (Last evaluated: May 8, 2012)

Review status:(0/4) 0 stars out of maximum of 4 stars

no assertion criteria provided

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000746892.1

Allele description [Variation Report for GRCh37/hg19 7q21.2(chr7:92317752-92449293)x3]

GRCh37/hg19 7q21.2(chr7:92317752-92449293)x3

Gene:
CDK6:cyclin dependent kinase 6 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
7q21.2
Genomic location:
Chr7: 92317752 - 92449293 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 7q21.2(chr7:92317752-92449293)x3
HGVS:

    Condition(s)

    Identifiers:
    MedGen: CN517202

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    Assertion and evidence details

    Submission AccessionSubmitterReview Status
    (Assertion method)
    Clinical Significance
    (Last evaluated)
    OriginMethodCitations
    SCV000875228Laboratory of Genetics and Genomics,Cincinnati Children's Hospital Medical Centerno assertion criteria providedBenign
    (May 8, 2012)
    unknownclinical testing

    Summary from all submissions

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

    Details of each submission

    From Laboratory of Genetics and Genomics,Cincinnati Children's Hospital Medical Center, SCV000875228.1

    #EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
    1not providednot providednot providednot providedclinical testing
    (GTR000295241.2)
    not provided
    #SampleMethodObservation
    OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
    1unknownunknownnot providedtissuenot provided
    (GTR000295241.2)
    not providednot providednot providednot provided

    Last Updated: Dec 17, 2019

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