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Variant : CV600246 (GRCh37/hg19 6p22.2(chr6:26110314-26338056)x3) Homo sapiens

Symbol: CV600246
Name: GRCh37/hg19 6p22.2(chr6:26110314-26338056)x3
Condition: not provided [RCV000745546]
Clinical Significance: benign
Last Evaluated: 04/09/2013
Review Status: no assertion criteria provided
Related Genes: H1-3   H1-4   H2AC6   H2AC7   H2AC8   H2BC10   H2BC4   H2BC5   H2BC6   H2BC7   H2BC8   H2BC9   H3C4   H3C6   H3C7   H3C8   H4C4   H4C5   H4C6   H4C7   H4C8   TRR-TCG4-1   TRX-CAT1-2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37626,110,314 - 26,338,056CLINVAR
Cytogenetic Map66p22.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14360911
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.