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GRCh37/hg19 Xp22.33(chrX:377908-582185)x3

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Interpretation:
Uncertain significance​

Review status:
no assertion criteria provided
Submissions:
1 (Most recent: Aug 16, 2018)
Last evaluated:
Nov 28, 2017
Accession:
VCV000564710.1
Variation ID:
564710
Description:
copy number gain
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GRCh37/hg19 Xp22.33(chrX:377908-582185)x3

Allele ID
555894
Variant type
copy number gain
Variant length
-
Cytogenetic location
Xp22.33
Genomic location
X: 377908-582185 (GRCh37) GRCh37 UCSC
HGVS
-
Protein change
-
Other names
-
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
-
Links
-
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Uncertain significance 1 no assertion criteria provided Nov 28, 2017 RCV000684199.1
Help No affected genes found.

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Uncertain significance
(Nov 28, 2017)
no assertion criteria provided
Method: clinical testing
not provided
Allele origin: germline
Quest Diagnostics Nichols Institute San Juan Capistrano
Accession: SCV000811708.1
Submitted: (Aug 16, 2018)
Evidence details

Citations for this variant

There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar.

Record last updated Aug 29, 2019