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Variant : CV165017 (GRCh38/hg38 13q33.2-34(chr13:104968135-114340331)x1) Homo sapiens

Symbol: CV165017
Name: GRCh38/hg38 13q33.2-34(chr13:104968135-114340331)x1
Condition: See cases [RCV000143330]
Clinical Significance: pathogenic
Last Evaluated: 01/09/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABHD13   ADPRHL1   ANKRD10   ANKRD10-IT1   ARGLU1   ARHGEF7   ARHGEF7-AS1   ARHGEF7-AS2   ATP11A   ATP11A-AS1   ATP11AUN   ATP4B   C13orf46   CARS2   CDC16   CFAP97D2   CHAMP1   COL4A1   COL4A2   COL4A2-AS1   COL4A2-AS2   CUL4A   DAOA   DAOA-AS1   DCUN1D2   EFNB2   F10   F10-AS1   F7   FAM155A   FAM155A-IT1   GAS6   GAS6-AS1   GAS6-DT   GRK1   GRTP1   GRTP1-AS1   ING1   IRS2   LAMP1   LIG4   LINC00343   LINC00346   LINC00354   LINC00368   LINC00370   LINC00396   LINC00399   LINC00431   LINC00443   LINC00452   LINC00454   LINC00460   LINC00551   LINC00552   LINC00565   LINC00567   LINC00676   LINC01043   LINC01044   LINC01054   LINC01070   LINC02337   LOC101928841   MCF2L   MCF2L-AS1   MIR1267   MIR4502   MIR548AR   MIR8073   MIR8075   MYO16   MYO16-AS1   NAXD   PCID2   PROZ   RAB20   RASA3   SNORD31B   SOX1   SOX1-OT   SPACA7   TEX29   TFDP1   TMCO3   TMEM255B   TNFSF13B   TUBGCP3   UPF3A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_104968135)_(114340331_?)del
NC_000013.10:g.(?_105620486)_(115085141_?)del
NC_000013.9:g.(?_104418487)_(114123908_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3813104,968,135 - 114,340,331CLINVAR
GRCh3713105,620,486 - 115,085,141 (+)CLINVAR
Build 3613104,418,487 - 114,123,908CLINVAR
Cytogenetic Map1313q33.2-34CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490928
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.