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Variant : CV162749 (GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3) Homo sapiens

Symbol: CV162749
Name: GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3
Condition: See cases [RCV000141497]
Clinical Significance: benign
Last Evaluated: 02/04/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABI1   ACBD5   ACBD7   ACBD7-DCLRE1CP1   AGAP4   AGAP9   AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   AL157895.1   AL358612.1   AL391839.1   AL606469.1   AL731567.1   ALOX5   ANKRD16   ANKRD26   ANKRD30A   ANTXRL   ANXA8   ANXA8L1   APBB1IP   ARHGAP12   ARHGAP21   ARL5B   ARMC3   ASB13   ATP5F1C   BAMBI   BEND7   BMI1   BMS1   C10orf126   C10orf67   C1QL3   CACNB2   CALML3   CALML3-AS1   CALML5   CAMK1D   CCDC3   CCDC7   CCNY   CDC123   CDNF   CELF2   CELF2-AS1   CELF2-AS2   CELF2-DT   COMMD3   COMMD3-BMI1   CREM   CSGALNACT2   CUBN   CUL2   CXCL12   DCLRE1C   DEPP1   DHTKD1   DNAJC1   EBLN1   ECHDC3   ENKUR   EPC1   FAM107B   FAM171A1   FAM238A   FAM238B   FAM238C   FAM245B   FAM25C   FAM25E   FAM25G   FBH1   FRMD4A   FXYD4   FZD8   GAD2   GATA3   GATA3-AS1   GDF10   GDF2   GDI2   GJD4   GPR158   GPR158-AS1   GPRIN2   HACD1   HNRNPF   HSPA14   HSPA14   IATPR   IL15RA   IL2RA   ITGA8   ITGB1   ITGB1-DT   ITIH2   ITIH5   JCAD   KIAA1217   KIF5B   KIN   LASTR   LINC00619   LINC00705   LINC00706   LINC00707   LINC00708   LINC00709   LINC00710   LINC00836   LINC00837   LINC00838   LINC00839   LINC00840   LINC00841   LINC00842   LINC00993   LINC00999   LINC01264   LINC01516   LINC01517   LINC01518   LINC02561   LINC02623   LINC02628   LINC02630   LINC02634   LINC02637   LINC02642   LINC02643   LINC02644   LINC02648   LINC02649   LINC02652   LINC02654   LINC02656   LINC02658   LINC02659   LINC02664   LINC02665   LINC02670   LINC02673   LINC02676   LINC02677   LINC02678   LINC02881   LINP1   LOC100130992   LOC100499489   LOC100505502   LOC101927699   LOC101928272   LOC101928453   LOC101929117   LOC101929279   LOC101929431   LOC102724593   LOC105376398   LOC105378269   LOC105378292   LOC105378577   LOC106736614   LOC106783505   LOC106783576   LOC107001062   LOC107275222   LOC107275223   LOC107275226   LOC108004524   LOC108353817   LOC108353819   LOC108903148   LOC108903149   LOC110121348   LOC110121355   LOC110121399   LOC110121405   LOC110121406   LOC110121476   LOC110121478   LOC110121502   LOC110121503   LOC110121506   LOC110121507   LOC111464994   LOC111501766   LOC111589212   LOC111818964   LOC111818965   LOC111818966   LOC111818967   LOC111946222   LOC111946223   LOC111946224   LOC111946225   LOC111946226   LOC111946227   LOC111946228   LOC111946229   LOC111946230   LOC111946231   LOC111946232   LOC111946234   LOC111946236   LOC111946237   LOC111946238   LOC111946239   LOC111946241   LOC111946242   LOC111946244   LOC111946245   LOC111946246   LOC111946251   LOC111946252   LOC114827857   LOC116216107   LOC116216108   LOC116216109   LOC116216110   LOC116216111   LOC116216112   LOC283028   LYZL1   LYZL2   MACORIS   MALRD1   MANCR   MAP3K8   MARCHF8   MASTL   MCM10   MCS+9.7   MEIG1   MINDY3   MIR1265   MIR1915   MIR1915HG   MIR3155A   MIR3155B   MIR3156-1   MIR3611   MIR4293   MIR4480   MIR4481   MIR4675   MIR4683   MIR5100   MIR511   MIR548AK   MIR548Q   MIR603   MIR604   MIR7162   MIR8086   MIR938   MKX   MKX-AS1   MLLT10   MPP7   MRC1   MSMB   MSRB2   MTPAP   MTRNR2L7   MYO3A   NCOA4   NEBL   NEBL-AS1   NET1   NMT2   NPY4R   NPY4R2   NRP1   NSUN6   NUDT5   ODAD2   OLAH   OPTN   OR13A1   OTUD1   PARD3   PARD3-AS1   PCAT5   PDSS1   PFKFB3   PHYH   PIP4K2A   PLXDC2   PRINS   PRKCQ   PRKCQ-AS1   PROSER2   PROSER2-AS1   PRPF18   PRTFDC1   PTCHD3   PTER   PTF1A   PTPN20   RAB18   RASGEF1A   RASSF4   RBM17   RBP3   RET   RPP38   RPP38-DT   RSU1   SEC61A2   SEPHS1   SFMBT2   SKIDA1   SLC39A12   SLC39A12-AS1   SNORA74C-1   SNORA86   SNORD129   SNORD130   SNORD3J   SPAG6   ST8SIA6   ST8SIA6-AS1   STAM   STAM-AS1   SUV39H2   SVIL   SVIL-AS1   SYT15   SYT15   TAF3   TASOR2   THNSL1   TIMM23   TMEM236   TMEM72   TMEM72-AS1   TRDMT1   TRN-GTT2-3   TRV-TAC3-1   TUBAL3   UCMA   UCN3   UPF2   USP6NL   USP6NL-AS1   VIM   VIM-AS1   WAC   WAC-AS1   WASHC2C   YME1L1   ZEB1   ZEB1-AS1   ZFAND4   ZNF22   ZNF22-AS1   ZNF239   ZNF248   ZNF25   ZNF32   ZNF32-AS1   ZNF32-AS2   ZNF32-AS3   ZNF33A   ZNF33B   ZNF37A   ZNF438   ZNF485   ZNF487   ZNF488  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_4604734)_(48074662_?)dup
NC_000010.10:g.(?_4646926)_(47531169_?)dup
NC_000010.9:g.(?_4636926)_(47125152_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38104,604,734 - 48,074,662CLINVAR
GRCh37104,646,926 - 47,531,169 (+)CLINVAR
Build 36104,636,926 - 47,125,152CLINVAR
Cytogenetic Map1010p15.1-q11.22CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489022
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.