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Variant : CV157730 (GRCh38/hg38 15q24.2-25.1(chr15:76006154-79982417)x1) Homo sapiens

Symbol: CV157730
Name: GRCh38/hg38 15q24.2-25.1(chr15:76006154-79982417)x1
Condition: See cases [RCV000137079]
Clinical Significance: pathogenic|uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACSBG1   ADAMTS7   ANKRD34C   ANKRD34C-AS1   BCL2A1   CHRNA3   CHRNA5   CHRNB4   CIB2   CRABP1   CTSH   DNAJA4   ETFA   HMG20A   HYKK   IDH3A   IREB2   ISL2   LINC00597   LINGO1   LINGO1-AS1   LINGO1-AS2   MINAR1   MIR184   MIR3713   MORF4L1   MTHFS   NRG4   PEAK1   PSMA4   PSTPIP1   RASGRF1   RCN2   SCAPER   SH2D7   ST20   ST20-AS1   ST20-MTHFS   TBC1D2B   TMED3   TMEM266   TRC-GCA5-1   TRK-CTT1-2   TSPAN3   WDR61  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_76006154)_(79982417_?)del
NC_000015.9:g.(?_76298495)_(80274759_?)del
NC_000015.8:g.(?_74085550)_(78061814_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381576,006,154 - 79,982,417CLINVAR
GRCh371576,298,495 - 80,274,759CLINVAR
Build 361574,085,550 - 78,061,814CLINVAR
Cytogenetic Map1515q24.2-25.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484638
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-08-06
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.