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Variant : CV676493 (GRCh37/hg19 6p22.2(chr6:26067079-26207758)x1) Homo sapiens

Symbol: CV676493
Name: GRCh37/hg19 6p22.2(chr6:26067079-26207758)x1
Condition: not provided [RCV000849592]
Clinical Significance: uncertain significance
Last Evaluated: 05/30/2017
Review Status: no assertion criteria provided
Related Genes: H1-4   H1-6   H2AC6   H2AC7   H2BC4   H2BC5   H2BC6   H2BC7   H3C4   H4C3   H4C4   H4C5   HFE  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37626,067,079 - 26,207,758CLINVAR
Cytogenetic Map66p22.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976640
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-11-12
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.