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GRCh37/hg19 17q25.1(chr17:72901452-73518861)x3 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 31, 2017
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000585184.3

Allele description [Variation Report for GRCh37/hg19 17q25.1(chr17:72901452-73518861)x3]

GRCh37/hg19 17q25.1(chr17:72901452-73518861)x3

Genes:
  • NT5C:5', 3'-nucleotidase, cytosolic [Gene - OMIM - HGNC]
  • ATP5PD:ATP synthase peripheral stalk subunit d [Gene - OMIM - HGNC]
  • CASKIN2:CASK interacting protein 2 [Gene - OMIM - HGNC]
  • HID1:HID1 domain containing [Gene - OMIM - HGNC]
  • JPT1:Jupiter microtubule associated homolog 1 [Gene - OMIM - HGNC]
  • MIF4GD:MIF4G domain containing [Gene - OMIM - HGNC]
  • USH1G:USH1 protein network component sans [Gene - OMIM - HGNC]
  • ARMC7:armadillo repeat containing 7 [Gene - HGNC]
  • CDR2L:cerebellar degeneration related protein 2 like [Gene - HGNC]
  • GGA3:golgi associated, gamma adaptin ear containing, ARF binding protein 3 [Gene - OMIM - HGNC]
  • GRB2:growth factor receptor bound protein 2 [Gene - OMIM - HGNC]
  • MRPL58:mitochondrial ribosomal protein L58 [Gene - OMIM - HGNC]
  • MRPS7:mitochondrial ribosomal protein S7 [Gene - OMIM - HGNC]
  • NUP85:nucleoporin 85 [Gene - OMIM - HGNC]
  • OTOP2:otopetrin 2 [Gene - OMIM - HGNC]
  • OTOP3:otopetrin 3 [Gene - OMIM - HGNC]
  • KCTD2:potassium channel tetramerization domain containing 2 [Gene - OMIM - HGNC]
  • SUMO2:small ubiquitin like modifier 2 [Gene - OMIM - HGNC]
  • SLC16A5:solute carrier family 16 member 5 [Gene - OMIM - HGNC]
  • SLC25A19:solute carrier family 25 member 19 [Gene - OMIM - HGNC]
  • TSEN54:tRNA splicing endonuclease subunit 54 [Gene - OMIM - HGNC]
  • TMEM94:transmembrane protein 94 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
17q25.1
Genomic location:
Chr17: 72901452 - 73518861 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 17q25.1(chr17:72901452-73518861)x3
HGVS:
    Observations:
    1

    Condition(s)

    Synonyms:
    none provided
    Identifiers:
    MedGen: CN517202

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    Assertion and evidence details

    Submission AccessionSubmitterReview Status
    (Assertion method)
    Clinical Significance
    (Last evaluated)
    OriginMethodCitations
    SCV000693399CeGaT Center for Human Genetics Tuebingen
    criteria provided, single submitter

    (Praxis fuer Humangenetik Tuebingen - Variant Classification Criteria)
    Uncertain significance
    (Oct 31, 2017)
    germlineclinical testing

    Citation Link

    Summary from all submissions

    EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
    not providedgermlineyes1not providednot providednot providednot providedclinical testing

    Details of each submission

    From CeGaT Center for Human Genetics Tuebingen, SCV000693399.4

    #EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
    1not provided1not providednot providedclinical testingnot provided
    #SampleMethodObservation
    OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
    1germlineyesnot providednot providednot provided1not providednot providednot provided

    Last Updated: Mar 26, 2023