U.S. flag

An official website of the United States government

GRCh37/hg19 7q22.1(chr7:102333119-103158261)x3 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 12, 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:
RCV000847426.2

Allele description [Variation Report for GRCh37/hg19 7q22.1(chr7:102333119-103158261)x3]

GRCh37/hg19 7q22.1(chr7:102333119-103158261)x3

Genes:
  • DNAJC2:DnaJ heat shock protein family (Hsp40) member C2 [Gene - OMIM - HGNC]
  • FBXL13:F-box and leucine rich repeat protein 13 [Gene - OMIM - HGNC]
  • NAPEPLD:N-acyl phosphatidylethanolamine phospholipase D [Gene - OMIM - HGNC]
  • ARMC10:armadillo repeat containing 10 [Gene - OMIM - HGNC]
  • FAM185A:family with sequence similarity 185 member A [Gene - HGNC]
  • LRRC17:leucine rich repeat containing 17 [Gene - OMIM - HGNC]
  • NFE4:nuclear factor, erythroid 4 [Gene - OMIM - HGNC]
  • PMPCB:peptidase, mitochondrial processing subunit beta [Gene - OMIM - HGNC]
  • PSMC2:proteasome 26S subunit, ATPase 2 [Gene - OMIM - HGNC]
  • RELN:reelin [Gene - OMIM - HGNC]
  • SLC26A5:solute carrier family 26 member 5 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
7q22.1
Genomic location:
Chr7: 102333119 - 103158261 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 7q22.1(chr7:102333119-103158261)x3
HGVS:

    Condition(s)

    Synonyms:
    none provided
    Identifiers:
    MedGen: CN517202

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...

    Assertion and evidence details

    Help
    Submission AccessionSubmitterReview Status
    (Assertion method)    		Clinical Significance
    (Last evaluated)    		OriginMethodCitations
    SCV000989548Bionano Laboratories
    no assertion criteria provided
    		Uncertain significance
    (Dec 12, 2017)     		unknownclinical testing

    Help

    Summary from all submissions

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

    Details of each submission

    From Bionano Laboratories, SCV000989548.1

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

    Last Updated: Dec 11, 2022