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GRCh37/hg19 7p22.3(chr7:967185-1781553)x3 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 13, 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:
RCV001259996.1

Allele description [Variation Report for GRCh37/hg19 7p22.3(chr7:967185-1781553)x3]

GRCh37/hg19 7p22.3(chr7:967185-1781553)x3

Genes:
  • ADAP1:ArfGAP with dual PH domains 1 [Gene - OMIM - HGNC]
  • GPER1:G protein-coupled estrogen receptor 1 [Gene - OMIM - HGNC]
  • GPR146:G protein-coupled receptor 146 [Gene - HGNC]
  • MAFK:MAF bZIP transcription factor K [Gene - OMIM - HGNC]
  • MICALL2:MICAL like 2 [Gene - HGNC]
  • UNCX:UNC homeobox [Gene - HGNC]
  • C7orf50:chromosome 7 open reading frame 50 [Gene - HGNC]
  • CYP2W1:cytochrome P450 family 2 subfamily W member 1 [Gene - OMIM - HGNC]
  • COX19:cytochrome c oxidase assembly factor COX19 [Gene - OMIM - HGNC]
  • ELFN1:extracellular leucine rich repeat and fibronectin type III domain containing 1 [Gene - OMIM - HGNC]
  • INTS1:integrator complex subunit 1 [Gene - OMIM - HGNC]
  • PSMG3:proteasome assembly chaperone 3 [Gene - OMIM - HGNC]
  • TMEM184A:transmembrane protein 184A [Gene - HGNC]
  • ZFAND2A:zinc finger AN1-type containing 2A [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
7p22.3
Genomic location:
Chr7: 967185 - 1781553 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 7p22.3(chr7:967185-1781553)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
    SCV001436965Quest Diagnostics Nichols Institute San Juan Capistrano
    no assertion criteria provided
    		Uncertain significance
    (Dec 13, 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, SCV001436965.1

    #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: Apr 23, 2022