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GRCh37/hg19 11p15.4(chr11:7837338-9295428)x3 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 28, 2017
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:
RCV000683357.1

Allele description [Variation Report for GRCh37/hg19 11p15.4(chr11:7837338-9295428)x3]

GRCh37/hg19 11p15.4(chr11:7837338-9295428)x3

Genes:
  • AKIP1:A-kinase interacting protein 1 [Gene - OMIM - HGNC]
  • DENND2B:DENN domain containing 2B [Gene - OMIM - HGNC]
  • DENND5A:DENN domain containing 5A [Gene - OMIM - HGNC]
  • LMO1:LIM domain only 1 [Gene - OMIM - HGNC]
  • NLRP10:NLR family pyrin domain containing 10 [Gene - OMIM - HGNC]
  • RIC3:RIC3 acetylcholine receptor chaperone [Gene - OMIM - HGNC]
  • TMEM9B:TMEM9 domain family member B [Gene - HGNC]
  • TUB:TUB bipartite transcription factor [Gene - OMIM - HGNC]
  • ASCL3:achaete-scute family bHLH transcription factor 3 [Gene - OMIM - HGNC]
  • C11orf16:chromosome 11 open reading frame 16 [Gene - HGNC]
  • EIF3F:eukaryotic translation initiation factor 3 subunit F [Gene - OMIM - HGNC]
  • NRIP3:nuclear receptor interacting protein 3 [Gene - OMIM - HGNC]
  • OR10A3:olfactory receptor family 10 subfamily A member 3 [Gene - HGNC]
  • OR10A6:olfactory receptor family 10 subfamily A member 6 (gene/pseudogene) [Gene - HGNC]
  • OR5P3:olfactory receptor family 5 subfamily P member 3 [Gene - HGNC]
  • RPL27A:ribosomal protein L27a [Gene - OMIM - HGNC]
  • STK33:serine/threonine kinase 33 [Gene - OMIM - HGNC]
  • SCUBE2:signal peptide, CUB domain and EGF like domain containing 2 [Gene - OMIM - HGNC]
  • SNORA3B:small nucleolar RNA, H/ACA box 3B [Gene - OMIM - HGNC]
  • TRIM66:tripartite motif containing 66 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
11p15.4
Genomic location:
Chr11: 7837338 - 9295428 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 11p15.4(chr11:7837338-9295428)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
    SCV000810865Quest Diagnostics Nichols Institute San Juan Capistrano
    no assertion criteria provided
    		Uncertain significance
    (Jun 28, 2017)     		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, SCV000810865.1

    #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