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Variant : CV156270 (GRCh38/hg38 13q31.3-32.1(chr13:93908109-94449189)x3) Homo sapiens

Symbol: CV156270
Name: GRCh38/hg38 13q31.3-32.1(chr13:93908109-94449189)x3
Condition: See cases [RCV000135798]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DCT   GPC6   GPC6-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_93908109)_(94449189_?)dup
NC_000013.10:g.(?_94560362)_(95101443_?)dup
NC_000013.9:g.(?_93358363)_(93899444_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381393,908,109 - 94,449,189CLINVAR
GRCh371394,560,362 - 95,101,443CLINVAR
Build 361393,358,363 - 93,899,444CLINVAR
Cytogenetic Map1313q31.3-32.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483364
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.