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Variant : CV600247 (GRCh37/hg19 6p22.2(chr6:26110961-26219744)x3) Homo sapiens

Symbol: CV600247
Name: GRCh37/hg19 6p22.2(chr6:26110961-26219744)x3
Condition: not provided [RCV000745547]
Clinical Significance: benign
Last Evaluated: 05/08/2012
Review Status: no assertion criteria provided
Related Genes: H1-4   H2AC6   H2AC7   H2AC8   H2BC4   H2BC5   H2BC6   H2BC7   H2BC8   H3C4   H4C4   H4C5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37626,110,961 - 26,219,744CLINVAR
Cytogenetic Map66p22.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14360912
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.