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Variant : CV163334 (GRCh38/hg38 13q31.3-32.1(chr13:93869283-94459255)x3) Homo sapiens

Symbol: CV163334
Name: GRCh38/hg38 13q31.3-32.1(chr13:93869283-94459255)x3
Condition: See cases [RCV000141918]
Clinical Significance: uncertain significance
Last Evaluated: 07/16/2013
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.(?_93869283)_(94459255_?)dup
NC_000013.10:g.(?_94521536)_(95111509_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381393,869,283 - 94,459,255CLINVAR
GRCh371394,521,536 - 95,111,509CLINVAR
Build 361393,319,537 - 93,909,510CLINVAR
Cytogenetic Map1313q31.3-32.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489440
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.