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GRCh38/hg38 Yq11.223(chrY:21891698-21922809)x3 AND See cases

Germline classification:
Benign (1 submission)
Last evaluated:
Apr 30, 2011
Review status:
Somatic classification
of clinical impact:
None
Review status:
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
no assertion criteria provided
Record status:
current
Accession:
RCV000140574.3

Allele description [Variation Report for GRCh38/hg38 Yq11.223(chrY:21891698-21922809)x3]

GRCh38/hg38 Yq11.223(chrY:21891698-21922809)x3

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 gain
Cytogenetic location:
Yq11.223
Genomic location:
Preferred name:
GRCh38/hg38 Yq11.223(chrY:21891698-21922809)x3
HGVS:
  • NC_000024.10:g.(?_21891698)_(21922809_?)dup
  • NC_000024.9:g.(?_24037845)_(24068956_?)dup
Links:
dbVar: nssv1609905; dbVar: nssv1609908; dbVar: nsv931780
Observations:
2

Condition(s)

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

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000181279GeneDx
no assertion criteria provided
Benign
(Apr 30, 2011)
not providedclinical testing

Last Updated: Apr 23, 2022

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