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Variant : CV596236 (GRCh37/hg19 21q22.11(chr21:31887658-32065821)x1) Homo sapiens

Symbol: CV596236
Name: GRCh37/hg19 21q22.11(chr21:31887658-32065821)x1
Condition: not provided [RCV000741536]
Clinical Significance: benign
Last Evaluated: 07/05/2012
Review Status: no assertion criteria provided
Related Genes: KRTAP19-6   KRTAP19-7   KRTAP20-1   KRTAP20-2   KRTAP20-3   KRTAP20-4   KRTAP22-1   KRTAP22-2   KRTAP6-1   KRTAP6-2   KRTAP6-3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372131,887,658 - 32,065,821CLINVAR
Cytogenetic Map2121q22.11CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14356910
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-11-17
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.