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GRCh37/hg19 19p13.3(chr19:4182912-4633772)x3 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 1, 2021
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:
RCV001833036.1

Allele description [Variation Report for GRCh37/hg19 19p13.3(chr19:4182912-4633772)x3]

GRCh37/hg19 19p13.3(chr19:4182912-4633772)x3

Genes:
  • EBI3:Epstein-Barr virus induced 3 [Gene - OMIM - HGNC]
  • MPND:MPN domain containing [Gene - HGNC]
  • SH3GL1:SH3 domain containing GRB2 like 1, endophilin A2 [Gene - OMIM - HGNC]
  • SHD:Src homology 2 domain containing transforming protein D [Gene - OMIM - HGNC]
  • UBXN6:UBX domain protein 6 [Gene - OMIM - HGNC]
  • YJU2:YJU2 splicing factor homolog [Gene - HGNC]
  • ANKRD24:ankyrin repeat domain 24 [Gene - HGNC]
  • CHAF1A:chromatin assembly factor 1 subunit A [Gene - OMIM - HGNC]
  • FSD1:fibronectin type III and SPRY domain containing 1 [Gene - OMIM - HGNC]
  • LRG1:leucine rich alpha-2-glycoprotein 1 [Gene - OMIM - HGNC]
  • PLIN4:perilipin 4 [Gene - OMIM - HGNC]
  • PLIN5:perilipin 5 [Gene - OMIM - HGNC]
  • SEMA6B:semaphorin 6B [Gene - OMIM - HGNC]
  • STAP2:signal transducing adaptor family member 2 [Gene - OMIM - HGNC]
  • TMIGD2:transmembrane and immunoglobulin domain containing 2 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
19p13.3
Genomic location:
Chr19: 4182912 - 4633772 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 19p13.3(chr19:4182912-4633772)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
    SCV002096273Quest Diagnostics Nichols Institute San Juan Capistrano
    no assertion criteria provided
    		Uncertain significance
    (Apr 1, 2021)     		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, SCV002096273.1

    #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