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Variant : CV437509 (GRCh37/hg19 11q24.1-25(chr11:122884694-134938470)x3) Homo sapiens

Symbol: CV437509
Name: GRCh37/hg19 11q24.1-25(chr11:122884694-134938470)x3
Condition: See cases [RCV000511146]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2015
Review Status: no assertion criteria provided
Related Genes: ACAD8   ACRV1   ADAMTS15   ADAMTS8   AP001993.1   APLP2   ARHGAP32   B3GAT1   BARX2   C11orf45   CCDC15   CDON   CHEK1   CLMP   DCPS   DDX25   EI24   ESAM   ETS1   FAM118B   FEZ1   FLI1   FOXRED1   GLB1L2   GLB1L3   GRAMD1B   HEPACAM   HEPN1   HSPA8   HYLS1   IGSF9B   JAM3   KCNJ1   KCNJ5   KIRREL3   LINC02714   LINC02743   LINC02873   MSANTD2   NCAPD3   NFRKB   NRGN   NTM   OPCML   OR10G4   OR10G7   OR10G8   OR10G9   OR10S1   OR4D5   OR6M1   OR6T1   OR6X1   OR8A1   OR8B12   OR8B2   OR8B3   OR8B4   OR8B8   OR8D1   OR8D2   OR8D4   OR8G1   OR8G2P   OR8G5   PANX3   PATE1   PATE2   PATE3   PATE4   PKNOX2   PRDM10   PUS3   ROBO3   ROBO4   RPUSD4   SCN3B   SIAE   SLC37A2   SNX19   SPA17   SPATA19   SRPRA   ST14   ST3GAL4   STT3A   TBRG1   THYN1   TIRAP   TMEM218   TMEM225   TMEM45B   TP53AIP1   VPS26B   VSIG2   VWA5A   ZBTB44   ZNF202  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3711122,884,694 - 134,938,470CLINVAR
Cytogenetic Map1111q24.1-25CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13444121
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE


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