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GRCh37/hg19 Yq11.223-11.23(chrY:25403868-27224389)x0 AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 11, 2020
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:
RCV001258430.1

Allele description [Variation Report for GRCh37/hg19 Yq11.223-11.23(chrY:25403868-27224389)x0]

GRCh37/hg19 Yq11.223-11.23(chrY:25403868-27224389)x0

Genes:
  • BPY2B:basic charge Y-linked 2B [Gene - HGNC]
  • BPY2C:basic charge Y-linked 2C [Gene - HGNC]
  • DAZ2:deleted in azoospermia 2 [Gene - OMIM - HGNC]
  • DAZ3:deleted in azoospermia 3 [Gene - OMIM - HGNC]
  • DAZ4:deleted in azoospermia 4 [Gene - OMIM - HGNC]
  • TTTY17B:testis-specific transcript, Y-linked 17B [Gene - HGNC]
  • TTTY3B:testis-specific transcript, Y-linked 3B [Gene - HGNC]
  • TTTY4B:testis-specific transcript, Y-linked 4B [Gene - HGNC]
  • TTTY4C:testis-specific transcript, Y-linked 4C [Gene - HGNC]
Variant type:
copy number loss
Cytogenetic location:
Yq11.223-11.23
Genomic location:
ChrY: 25403868 - 27224389 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 Yq11.223-11.23(chrY:25403868-27224389)x0
HGVS:
NC_000024.9:g.(?_25403868)_(27224389_?)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
SCV001435399Quest Diagnostics Nichols Institute San Juan Capistrano
no assertion criteria provided
Uncertain significance
(Mar 11, 2020) 		germlineclinical testing

Help

Summary from all submissions

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

Details of each submission

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV001435399.1

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

Last Updated: Apr 23, 2022