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Variant : CV161996 (GRCh38/hg38 21q21.3(chr21:26892213-28034654)x3) Homo sapiens

Symbol: CV161996
Name: GRCh38/hg38 21q21.3(chr21:26892213-28034654)x3
Condition: See cases [RCV000140837]
Clinical Significance: uncertain significance
Last Evaluated: 01/09/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAMTS5   LINC00113   LINC00314   LINC01673   LOC110121429   MIR4759  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_26892213)_(28034654_?)dup
NC_000021.8:g.(?_28264532)_(29406973_?)dup
NC_000021.7:g.(?_27186403)_(28328844_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382126,892,213 - 28,034,654CLINVAR
GRCh372128,264,532 - 29,406,973CLINVAR
Build 362127,186,403 - 28,328,844CLINVAR
Cytogenetic Map2121q21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488365
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.