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Variant : CV158017 (GRCh38/hg38 21q22.3(chr21:41733640-46671060)x1) Homo sapiens

Symbol: CV158017
Name: GRCh38/hg38 21q22.3(chr21:41733640-46671060)x1
Condition: See cases [RCV000137341]
Clinical Significance: pathogenic
Last Evaluated: 02/08/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AATBC   ABCG1   ADARB1   AGPAT3   AIRE   AP001625.3   C21orf58   C2CD2   CBS   CFAP410   COL18A1   COL18A1-AS1   COL18A1-AS2   COL6A1   COL6A2   CRYAA   CSTB   DIP2A   DIP2A-IT1   DNMT3L   DNMT3L-AS1   ERVH48-1   FAM207A   FRGCA   FTCD   FTCD-AS1   GATD3A   H2BS1   HSF2BP   ICOSLG   ITGB2   ITGB2-AS1   KRTAP10-1   KRTAP10-10   KRTAP10-11   KRTAP10-12   KRTAP10-2   KRTAP10-3   KRTAP10-4   KRTAP10-5   KRTAP10-6   KRTAP10-7   KRTAP10-8   KRTAP10-9   KRTAP12-1   KRTAP12-2   KRTAP12-3   KRTAP12-4   LINC00163   LINC00205   LINC00313   LINC00315   LINC00316   LINC00319   LINC00322   LINC00334   LINC01424   LINC01547   LINC01668   LINC01671   LINC01678   LINC01679   LINC01694   LINC02575   LOC101928796   LOC108251799   LOC108254685   LOC108281139   LOC108281151   LOC109029533   LOC110121500   LOC112694749   LOC112694750   LOC112694751   LOC112694752   LOC112694753   LOC112694754   LOC114004360   LOC116309124   LOC116309125   LRRC3   LRRC3-DT   LSS   MCM3AP   MCM3AP-AS1   MIR5692B   MIR6070   MIR6814   MIR6815   NDUFV3   PCBP3   PCBP3-AS1   PCNT   PDE9A   PDE9A-AS1   PDXK   PFKL   PICSAR   PKNOX1   POFUT2   PRDM15   PRMT2   PTTG1IP   PWP2   RIPK4   RRP1   RRP1B   RSPH1   S100B   SIK1   SLC19A1   SLC37A1   SNORA91   SNORD159   SPATC1L   SUMO3   TFF1   TFF2   TFF3   TMPRSS3   TRAPPC10   TRPM2   TRPM2-AS   TSPEAR   TSPEAR-AS1   TSPEAR-AS2   U2AF1   UBASH3A   UBE2G2   UMODL1   UMODL1-AS1   WDR4   YBEY   ZBTB21   ZNF295-AS1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_41733640)_(46671060_?)del
Human AssemblyChrPosition (strand)Source
GRCh382141,733,640 - 46,671,060CLINVAR
GRCh372143,153,800 - 48,090,972CLINVAR
Build 362142,026,869 - 46,915,400CLINVAR
Cytogenetic Map2121q22.3CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9484898
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
Status: ACTIVE


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