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Variant : CV804367 (GRCh37/hg19 21q22.11(chr21:31711916-34632473)x1) Homo sapiens

Symbol: CV804367
Name: GRCh37/hg19 21q22.11(chr21:31711916-34632473)x1
Condition: not provided [RCV001007125]
Clinical Significance: pathogenic
Last Evaluated: 10/05/2018
Review Status: no assertion criteria provided
Related Genes: C21orf62   CFAP298   EVA1C   HUNK   IFNAR2   KRTAP11-1   KRTAP13-1   KRTAP13-2   KRTAP13-3   KRTAP13-4   KRTAP15-1   KRTAP19-1   KRTAP19-2   KRTAP19-3   KRTAP19-4   KRTAP19-5   KRTAP19-6   KRTAP19-7   KRTAP19-8   KRTAP20-1   KRTAP20-2   KRTAP20-3   KRTAP20-4   KRTAP21-1   KRTAP21-2   KRTAP21-3   KRTAP22-1   KRTAP22-2   KRTAP23-1   KRTAP6-1   KRTAP6-2   KRTAP6-3   KRTAP7-1   KRTAP8-1   MIS18A   MRAP   OLIG1   OLIG2   PAXBP1   SCAF4   SOD1   SYNJ1   TCP10L   TIAM1   URB1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372131,711,916 - 34,632,473CLINVAR
Cytogenetic Map2121q22.11CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25316898
Created: 2020-04-07
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.