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Variant : CV804360 (GRCh37/hg19 21q21.3-22.11(chr21:27826100-32468109)x1) Homo sapiens

Symbol: CV804360
Name: GRCh37/hg19 21q21.3-22.11(chr21:27826100-32468109)x1
Condition: not provided [RCV001007118]
Clinical Significance: pathogenic
Last Evaluated: 11/15/2018
Review Status: no assertion criteria provided
Related Genes: ADAMTS1   ADAMTS5   BACH1   CCT8   CLDN17   CLDN8   CYYR1   GRIK1   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   KRTAP24-1   KRTAP25-1   KRTAP26-1   KRTAP27-1   KRTAP6-1   KRTAP6-2   KRTAP6-3   KRTAP7-1   KRTAP8-1   LTN1   MAP3K7CL   N6AMT1   RWDD2B   USP16  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh372127,826,100 - 32,468,109CLINVAR
Cytogenetic Map2121q21.3-22.11CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 25316886
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.