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GRCh37/hg19 Yp11.2(chrY:9417393-9882301)x2 AND See cases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 14, 2016
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000239405.2

Allele description [Variation Report for GRCh37/hg19 Yp11.2(chrY:9417393-9882301)x2]

GRCh37/hg19 Yp11.2(chrY:9417393-9882301)x2

Genes:
  • TTTY1:testis-specific transcript, Y-linked 1 [Gene - HGNC]
  • TTTY21:testis-specific transcript, Y-linked 21 [Gene - HGNC]
  • TTTY22:testis-specific transcript, Y-linked 22 [Gene - HGNC]
  • TTTY23:testis-specific transcript, Y-linked 23 [Gene - HGNC]
  • TTTY2:testis-specific transcript, Y-linked 2 [Gene - HGNC]
  • TTTY7B:testis-specific transcript, Y-linked 7B [Gene - HGNC]
  • TTTY8:testis-specific transcript, Y-linked 8 [Gene - HGNC]
Variant type:
copy number gain
Cytogenetic location:
Yp11.2
Genomic location:
ChrY: 9417393 - 9882301 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 Yp11.2(chrY:9417393-9882301)x2
HGVS:
    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
    SCV000297790Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington
    criteria provided, single submitter

    (Clinical Cytogenomics Laboratory Policy on CNV Interpretation)    		Uncertain significance
    (Jun 14, 2016)     		unknownclinical testing

    Citation Link

    Help

    Summary from all submissions

    EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
    not providedunknownyes11not providednot providednot providedclinical testing

    Details of each submission

    From Clinical Genomics Laboratory, Laboratory for Precision Diagnostics, University of Washington, SCV000297790.2

    #EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
    1not provided1not providednot providedclinical testingnot provided

    Description

    Patient also had 4q35.2(189,737,788-190,963,766)x1

    #SampleMethodObservation
    OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
    1unknownyesnot providedUmbilical Cord Bloodnot provided1not provided1not provided

    Last Updated: Dec 24, 2022