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GRCh38/hg38 Yq11.223(chrY:21880447-21922809)x1 AND See cases

Germline classification:
Benign (1 submission)
Last evaluated:
Apr 30, 2011
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:
RCV000140583.3

Allele description [Variation Report for GRCh38/hg38 Yq11.223(chrY:21880447-21922809)x1]

GRCh38/hg38 Yq11.223(chrY:21880447-21922809)x1

Genes:
RBMY1D:RNA binding motif protein Y-linked family 1 member D [Gene - HGNC]
RBMY1E:RNA binding motif protein Y-linked family 1 member E [Gene - HGNC]
Variant type:
copy number loss
Cytogenetic location:
Yq11.223
Genomic location:
Preferred name:
GRCh38/hg38 Yq11.223(chrY:21880447-21922809)x1
HGVS:
  • NC_000024.10:g.(?_21880447)_(21922809_?)del
  • NC_000024.8:g.(?_22435982)_(22478344_?)del
  • NC_000024.9:g.(?_24026594)_(24068956_?)del
Links:
dbVar: nssv1609933; dbVar: nsv931790
Observations:
1

Condition(s)

Name:
See cases [See the Variation display for details]
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000181290GeneDx
no assertion criteria provided
Benign
(Apr 30, 2011) 		not providedclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot providedyes1not providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000181290.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not providedyesnot providednot providedDiscovery1not providednot providednot provided

Last Updated: Apr 23, 2022