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GRCh37/hg19 9q31.3-32(chr9:113673200-115935268)x1 AND See cases

Germline classification:
Uncertain significance (1 submission)
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:
RCV002286355.1

Allele description [Variation Report for GRCh37/hg19 9q31.3-32(chr9:113673200-115935268)x1]

GRCh37/hg19 9q31.3-32(chr9:113673200-115935268)x1

Genes:
  • DNAJC25-GNG10:DNAJC25-GNG10 readthrough [Gene - HGNC]
  • DNAJC25:DnaJ heat shock protein family (Hsp40) member C25 [Gene - HGNC]
  • ECPAS:Ecm29 proteasome adaptor and scaffold [Gene - OMIM - HGNC]
  • FKBP15:FKBP prolyl isomerase family member 15 [Gene - OMIM - HGNC]
  • GNG10:G protein subunit gamma 10 [Gene - OMIM - HGNC]
  • INIP:INTS3 and NABP interacting protein [Gene - OMIM - HGNC]
  • KIAA1958:KIAA1958 [Gene - OMIM - HGNC]
  • UGCG:UDP-glucose ceramide glucosyltransferase [Gene - OMIM - HGNC]
  • ZFP37:ZFP37 zinc finger protein [Gene - OMIM - HGNC]
  • HSDL2:hydroxysteroid dehydrogenase like 2 [Gene - HGNC]
  • LPAR1:lysophosphatidic acid receptor 1 [Gene - OMIM - HGNC]
  • OR2K2:olfactory receptor family 2 subfamily K member 2 [Gene - HGNC]
  • PTBP3:polypyrimidine tract binding protein 3 [Gene - OMIM - HGNC]
  • PTGR1:prostaglandin reductase 1 [Gene - OMIM - HGNC]
  • SHOC1:shortage in chiasmata 1 [Gene - OMIM - HGNC]
  • SLC31A2:solute carrier family 31 member 2 [Gene - OMIM - HGNC]
  • SLC46A2:solute carrier family 46 member 2 [Gene - OMIM - HGNC]
  • SNX30:sorting nexin family member 30 [Gene - HGNC]
  • SUSD1:sushi domain containing 1 [Gene - HGNC]
  • ZNF483:zinc finger protein 483 [Gene - HGNC]
  • ZNF883:zinc finger protein 883 [Gene - HGNC]
Variant type:
copy number loss
Cytogenetic location:
9q31.3-32
Genomic location:
Chr9: 113673200 - 115935268 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 9q31.3-32(chr9:113673200-115935268)x1
HGVS:

    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
    SCV002575076Cytogenetics, Genetics Associates, Inc.
    no assertion criteria provided
    		Uncertain significanceunknownclinical testing

    Help

    Summary from all submissions

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

    Details of each submission

    From Cytogenetics, Genetics Associates, Inc., SCV002575076.1

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

    Last Updated: Mar 26, 2023