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Variant : CV556402 (GRCh37/hg19 1q32.2(chr1:210026523-211033868)x3) Homo sapiens

Symbol: CV556402
Name: GRCh37/hg19 1q32.2(chr1:210026523-211033868)x3
Condition: not provided [RCV000684693]
Clinical Significance: uncertain significance
Last Evaluated: 11/03/2017
Review Status: no assertion criteria provided
Related Genes: HHAT   KCNH1   SERTAD4   SYT14   UTP25  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371210,026,523 - 211,033,868CLINVAR
Cytogenetic Map11q32.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798935
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-10-01
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.