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GRCh37/hg19 9q33.2-33.3(chr9:125349988-126462569)x1 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 10, 2018
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:
RCV000849649.2

Allele description [Variation Report for GRCh37/hg19 9q33.2-33.3(chr9:125349988-126462569)x1]

GRCh37/hg19 9q33.2-33.3(chr9:125349988-126462569)x1

Genes:
  • DENND1A:DENN domain containing 1A [Gene - OMIM - HGNC]
  • GPR21:G protein-coupled receptor 21 [Gene - OMIM - HGNC]
  • RABGAP1:RAB GTPase activating protein 1 [Gene - OMIM - HGNC]
  • CRB2:crumbs cell polarity complex component 2 [Gene - OMIM - HGNC]
  • OR1B1:olfactory receptor family 1 subfamily B member 1 [Gene - HGNC]
  • OR1K1:olfactory receptor family 1 subfamily K member 1 [Gene - HGNC]
  • OR1L1:olfactory receptor family 1 subfamily L member 1 [Gene - HGNC]
  • OR1L3:olfactory receptor family 1 subfamily L member 3 [Gene - HGNC]
  • OR1L4:olfactory receptor family 1 subfamily L member 4 [Gene - HGNC]
  • OR1L6:olfactory receptor family 1 subfamily L member 6 [Gene - HGNC]
  • OR1Q1:olfactory receptor family 1 subfamily Q member 1 [Gene - HGNC]
  • OR5C1:olfactory receptor family 5 subfamily C member 1 [Gene - HGNC]
  • PDCL:phosducin like [Gene - OMIM - HGNC]
  • RC3H2:ring finger and CCCH-type domains 2 [Gene - OMIM - HGNC]
  • STRBP:spermatid perinuclear RNA binding protein [Gene - OMIM - HGNC]
  • ZBTB26:zinc finger and BTB domain containing 26 [Gene - OMIM - HGNC]
  • ZBTB6:zinc finger and BTB domain containing 6 [Gene - OMIM - HGNC]
Variant type:
copy number loss
Cytogenetic location:
9q33.2-33.3
Genomic location:
Chr9: 125349988 - 126462569 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 9q33.2-33.3(chr9:125349988-126462569)x1
HGVS:
NC_000009.11:g.(?_125349988)_(126462569_?)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
SCV000991791Bionano Laboratories
no assertion criteria provided
Uncertain significance
(Apr 10, 2018) 		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, SCV000991791.1

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

Last Updated: Mar 26, 2023