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GRCh37/hg19 17p11.2(chr17:18529674-18923470)x1 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 18, 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:
RCV000848947.2

Allele description [Variation Report for GRCh37/hg19 17p11.2(chr17:18529674-18923470)x1]

GRCh37/hg19 17p11.2(chr17:18529674-18923470)x1

Genes:
  • FBXW10:F-box and WD repeat domain containing 10 [Gene - OMIM - HGNC]
  • TBC1D28:TBC1 domain family member 28 [Gene - HGNC]
  • FAM83G:family with sequence similarity 83 member G [Gene - OMIM - HGNC]
  • PRPSAP2:phosphoribosyl pyrophosphate synthetase associated protein 2 [Gene - OMIM - HGNC]
  • SLC5A10:solute carrier family 5 member 10 [Gene - OMIM - HGNC]
  • TVP23B:trans-golgi network vesicle protein 23 homolog B [Gene - HGNC]
  • TRIM16L:tripartite motif containing 16 like [Gene - HGNC]
Variant type:
copy number loss
Cytogenetic location:
17p11.2
Genomic location:
Chr17: 18529674 - 18923470 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 17p11.2(chr17:18529674-18923470)x1
HGVS:
NC_000017.10:g.(?_18529674)_(18923470_?)del

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
SCV000991089Bionano Laboratories
no assertion criteria provided
Uncertain significance
(Aug 18, 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, SCV000991089.1

#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