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GRCh37/hg19 7q31.1(chr7:109594999-113885203)x3 AND not provided

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jan 21, 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:
RCV001005995.1

Allele description [Variation Report for GRCh37/hg19 7q31.1(chr7:109594999-113885203)x3]

GRCh37/hg19 7q31.1(chr7:109594999-113885203)x3

Genes:
  • GPR85:G protein-coupled receptor 85 [Gene - OMIM - HGNC]
  • BMT2:base methyltransferase of 25S rRNA 2 homolog [Gene - OMIM - HGNC]
  • DOCK4:dedicator of cytokinesis 4 [Gene - OMIM - HGNC]
  • FOXP2:forkhead box P2 [Gene - OMIM - HGNC]
  • IMMP2L:inner mitochondrial membrane peptidase subunit 2 [Gene - OMIM - HGNC]
  • IFRD1:interferon related developmental regulator 1 [Gene - OMIM - HGNC]
  • LRRN3:leucine rich repeat neuronal 3 [Gene - OMIM - HGNC]
  • LSMEM1:leucine rich single-pass membrane protein 1 [Gene - HGNC]
  • PPP1R3A:protein phosphatase 1 regulatory subunit 3A [Gene - OMIM - HGNC]
  • TMEM168:transmembrane protein 168 [Gene - HGNC]
  • ZNF277:zinc finger protein 277 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
7q31.1
Genomic location:
Chr7: 109594999 - 113885203 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 7q31.1(chr7:109594999-113885203)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
    SCV001165553Quest Diagnostics Nichols Institute San Juan Capistrano
    no assertion criteria provided
    		Likely pathogenic
    (Jan 21, 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, SCV001165553.1

    #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