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Variant : CV158578 (GRCh38/hg38 13q12.11-14.11(chr13:19671934-40914767)x3) Homo sapiens

Symbol: CV158578
Name: GRCh38/hg38 13q12.11-14.11(chr13:19671934-40914767)x3
Condition: See cases [RCV000137892]
Clinical Significance: pathogenic
Last Evaluated: 10/26/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ALG5   ALOX5AP   AMER2   ATP12A   ATP8A2   B3GLCT   BRCA2   C1QTNF9   C1QTNF9B   CCDC169   CCDC169-SOHLH2   CCNA1   CDK8   CDX2   CENPJ   COG6   CRYL1   CSNK1A1L   DCLK1   EEF1AKMT1   EXOSC8   FGF9   FLT1   FLT3   FOXO1   FREM2   FREM2-AS1   FRY   FRY-AS1   GJA3   GJB2   GJB6   GPR12   GSX1   GTF3A   HMGB1   HSPH1   IFT88   IL17D   KATNAL1   KL   LATS2   LHFPL6   LINC00297   LINC00327   LINC00332   LINC00365   LINC00366   LINC00367   LINC00384   LINC00385   LINC00398   LINC00412   LINC00415   LINC00423   LINC00424   LINC00426   LINC00437   LINC00445   LINC00457   LINC00463   LINC00539   LINC00540   LINC00543   LINC00544   LINC00545   LINC00547   LINC00548   LINC00566   LINC00571   LINC00572   LINC00598   LINC00621   LINC01046   LINC01048   LINC01053   LINC01058   LINC01072   LINC02340   LINC02343   LINC02344   LNX2   MAB21L1   MEDAG   MICU2   MIPEP   MIR2276   MIR320D1   MIR4305   MIR4499   MIR621   MPHOSPH8   MRPL57   MRPS31   MTIF3   MTMR6   MTUS2   MTUS2-AS1   N4BP2L1   N4BP2L2   N4BP2L2-IT2   NBEA   NHLRC3   NUP58   PABPC3   PAN3   PAN3-AS1   PARP4   PCOTH   PDS5B   PDX1   PLUT   POLR1D   POMP   POSTN   PROSER1   PSPC1   RASL11A   RFC3   RFXAP   RNF17   RNF6   RPL21   RXFP2   SACS   SACS-AS1   SAP18   SERTM1   SGCG   SHISA2   SKA3   SLC25A15   SLC46A3   SLC7A1   SMAD9   SNORA27   SNORD102   SOHLH2   SPART   SPART-AS1   SPATA13   SPATA13-AS1   STARD13   STARD13-AS   STOML3   SUPT20H   TEX26   TEX26-AS1   TNFRSF19   TRN-GTT2-4   TRPC4   UBE2L5   UBL3   UFM1   URAD   USP12   USP12-AS1   USP12-AS2   USPL1   WASF3   XPO4   ZAR1L   ZDHHC20   ZMYM2   ZMYM5  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_19671934)_(40914767_?)dup
Human AssemblyChrPosition (strand)Source
GRCh381319,671,934 - 40,914,767CLINVAR
GRCh371320,246,074 - 41,488,903CLINVAR
Build 361319,144,074 - 40,386,903CLINVAR
Cytogenetic Map1313q12.11-14.11CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9485443
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE


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