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Variant : CV71625 (GRCh38/hg38 21q21.3-22.11(chr21:29850105-30680142)x3) Homo sapiens

Symbol: CV71625
Name: GRCh38/hg38 21q21.3-22.11(chr21:29850105-30680142)x3
Condition: See cases [RCV000050615]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: CLDN17   CLDN8   GRIK1   KRTAP13-1   KRTAP13-2   KRTAP13-3   KRTAP13-4   KRTAP15-1   KRTAP19-1   KRTAP19-2   KRTAP19-3   KRTAP19-4   KRTAP19-5   KRTAP19-6   KRTAP19-7   KRTAP20-1   KRTAP20-2   KRTAP20-3   KRTAP20-4   KRTAP22-1   KRTAP22-2   KRTAP23-1   KRTAP24-1   KRTAP25-1   KRTAP26-1   KRTAP27-1   KRTAP6-1   KRTAP6-2   KRTAP6-3   LINC00307   MIR4327  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_29850105)_(30680142_?)dup
Human AssemblyChrPosition (strand)Source
GRCh382129,850,105 - 30,680,142CLINVAR
GRCh372131,222,422 - 32,052,460CLINVAR
Build 362130,144,293 - 30,974,331CLINVAR
Cytogenetic Map2121q21.3-22.11CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 8617723
Created: 2014-05-13
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.