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GRCh37/hg19 8q11.23(chr8:52605905-54913501)x3 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 29, 2019
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:
RCV001258408.1

Allele description [Variation Report for GRCh37/hg19 8q11.23(chr8:52605905-54913501)x3]

GRCh37/hg19 8q11.23(chr8:52605905-54913501)x3

Genes:
  • ALKAL1:ALK and LTK ligand 1 [Gene - OMIM - HGNC]
  • ATP6V1H:ATPase H+ transporting V1 subunit H [Gene - OMIM - HGNC]
  • RB1CC1:RB1 inducible coiled-coil 1 [Gene - OMIM - HGNC]
  • ST18:ST18 C2H2C-type zinc finger transcription factor [Gene - OMIM - HGNC]
  • NPBWR1:neuropeptides B and W receptor 1 [Gene - OMIM - HGNC]
  • OPRK1:opioid receptor kappa 1 [Gene - OMIM - HGNC]
  • PXDNL:peroxidasin like [Gene - OMIM - HGNC]
  • PCMTD1:protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 [Gene - OMIM - HGNC]
  • RGS20:regulator of G protein signaling 20 [Gene - OMIM - HGNC]
  • TCEA1:transcription elongation factor A1 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
8q11.23
Genomic location:
Chr8: 52605905 - 54913501 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 8q11.23(chr8:52605905-54913501)x3
HGVS:

    Condition(s)

    Synonyms:
    none provided
    Identifiers:
    MedGen: CN517202

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    Assertion and evidence details

    Help
    Submission AccessionSubmitterReview Status
    (Assertion method)    		Clinical Significance
    (Last evaluated)    		OriginMethodCitations
    SCV001435377Quest Diagnostics Nichols Institute San Juan Capistrano
    no assertion criteria provided
    		Uncertain significance
    (Aug 29, 2019)     		germlineclinical testing

    Help

    Summary from all submissions

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

    Details of each submission

    From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV001435377.1

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

    Last Updated: Oct 14, 2023