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Variant : CV600282 (GRCh37/hg19 6p22.1(chr6:27713299-27872832)x3) Homo sapiens

Symbol: CV600282
Name: GRCh37/hg19 6p22.1(chr6:27713299-27872832)x3
Condition: not provided [RCV000745582]
Clinical Significance: benign
Last Evaluated: 02/08/2011
Review Status: no assertion criteria provided
Related Genes: H1-5   H2AC13   H2AC14   H2AC15   H2AC16   H2AC17   H2BC13   H2BC14   H2BC15   H2BC17   H3C10   H3C11   H3C12   H4C11   H4C12   H4C13   TRX-CAT2-1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37627,713,299 - 27,872,832CLINVAR
Cytogenetic Map66p22.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14360947
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-08
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.