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Variant : CV676727 (GRCh37/hg19 9p13.3-q13(chr9:34542635-68210033)x3) Homo sapiens

Symbol: CV676727
Name: GRCh37/hg19 9p13.3-q13(chr9:34542635-68210033)x3
Condition: not provided [RCV000849826]
Clinical Significance: pathogenic
Last Evaluated: 09/27/2017
Review Status: no assertion criteria provided
Related Genes: ALDH1B1   ANKRD18A   ANKRD20A1   ARHGEF39   ARID3C   C9orf131   CA9   CCDC107   CCIN   CCL19   CCL21   CCL27   CD72   CLTA   CNTFR   CNTNAP3   CNTNAP3B   CREB3   DCAF10   DCTN3   DNAJB5   EXOSC3   FAM166B   FAM205A   FAM214B   FAM221B   FAM27D1   FANCG   FBXO10   FRMPD1   GALT   GBA2   GLIPR2   GNE   GRHPR   HINT2   HRCT1   IGFBPL1   IL11RA   MELK   MSMP   NPR2   OR13J1   OR2S2   PAX5   PHF24   PIGO   POLR1E   RECK   RGP1   RMRP   RNF38   RPP25L   RUSC2   SHB   SIGMAR1   SIT1   SLC25A51   SPAG8   SPATA31A1   SPATA31A3   SPATA31A5   SPATA31A6   SPATA31A7   STOML2   TESK1   TLN1   TMEM8B   TOMM5   TPM2   TRMT10B   UNC13B   VCP   ZBTB5   ZCCHC7   ZNF658  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37934,542,635 - 68,210,033CLINVAR
Cytogenetic Map99p13.3-q13CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14981321
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-21
Status: ACTIVE


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