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Variant : CV602294 (GRCh37/hg19 8q12.1(chr8:59446454-59523394)x3) Homo sapiens

Symbol: CV602294
Name: GRCh37/hg19 8q12.1(chr8:59446454-59523394)x3
Condition: not provided [RCV000747594]
Clinical Significance: benign
Last Evaluated: 11/08/2012
Review Status: no assertion criteria provided
Related Genes: NSMAF   SDCBP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37859,446,454 - 59,523,394CLINVAR
Cytogenetic Map88q12.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14362939
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-07
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.