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GRCh37/hg19 Xp22.33-q28(chrX:1-155270560) AND Turner syndrome

Germline classification:
Pathogenic (1 submission)
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:
RCV002280668.1

Allele description [Variation Report for GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)]

GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)

Genes:
Variant type:
copy number loss
Cytogenetic location:
Xp22.33-q28
Genomic location:
ChrX: 1 - 155270560 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)
Observations:
1

Condition(s)

Name:
Turner syndrome (MX)
Synonyms:
Ullrich-Turner syndrome; Bonnevie-Ulrich syndrome; Schereshevkii Turner Syndrome; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0019499; MedGen: C0041408

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002568931Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital
no assertion criteria provided
Pathogenicunknown, germlineclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot provided1not providedclinical testing
not providedunknownyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital, SCV002568931.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
2not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided
2germlineyes1not providednot provided1not providednot providednot provided

Last Updated: Mar 26, 2023