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46;XY;t(1;6)(q23;q13)dn

Variation ID: Help
267836
Review status: Help
criteria provided, single submitter1 star out of maximum of 4 stars

Interpretation Help

Clinical significance:
Uncertain significance
Last evaluated:
Aug 20, 2016
Number of submission(s):
1
Condition(s):
See supporting ClinVar records

Allele(s) Help

46;XY;t(1;6)(q23;q13)dn

Allele ID:
263212
Variant type:
Translocation
Cytogenetic location:
1q23

Variant frequency in dbGaP Help

No dbGaP data has been submitted for this variant.

Assertion and evidence details

Germline

Clinical significance
(Last evaluated)
Review status
(Assertion method)
Collection methodCondition(s)
(Mode of inheritance)
OriginCitationsSubmitter - Study nameSubmission accession
Uncertain significance
(Aug 20, 2016)
criteria provided, single submitter
researchde novoTalkowski Laboratory, Center for Human Genetic Research,Massachusetts General Hospital
Study description
SCV000320784.1
SubmitterFamiliesIndividualsAllele originEthnicityGeographic originCitations and DatabasesDescription
Talkowski Laboratory, Center for Human Genetic Research,Massachusetts General Hospitalnot providednot providedde novonot providednot providednot provided
SubmitterAllele originIndividualsPhenotypes (Affected status)EthnicityGeographic originCitationsDescription

Last Updated: Mar 31, 2019

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