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Variant : CV555660 (GRCh37/hg19 17q25.3(chr17:76552611-81041938)x3) Homo sapiens

Symbol: CV555660
Name: GRCh37/hg19 17q25.3(chr17:76552611-81041938)x3
Condition: not provided [RCV000683965]
Clinical Significance: likely pathogenic
Last Evaluated: 10/20/2017
Review Status: no assertion criteria provided
Related Genes: AATK   ACTG1   ALYREF   ANAPC11   ARHGDIA   ARL16   ASPSCR1   B3GNTL1   BAHCC1   BAIAP2   C1QTNF1   CANT1   CARD14   CBX2   CBX4   CBX8   CCDC137   CCDC40   CCDC57   CD7   CENPX   CEP131   CHMP6   CSNK1D   CYBC1   CYTH1   DCXR   DNAH17   DUS1L   EIF4A3   ENDOV   ENGASE   ENPP7   FAAP100   FASN   FN3K   FN3KRP   FOXK2   FSCN2   GAA   GCGR   GPS1   HEXD   HEXD-IT1   HGS   LGALS3BP   LRRC45   MAFG   MCRIP1   METRNL   MIR338   MRPL12   MYADML2   NARF   NDUFAF8   NOTUM   NPB   NPLOC4   NPTX1   OGFOD3   OXLD1   P4HB   PCYT2   PDE6G   PPP1R27   PYCR1   RAB40B   RAC3   RBFOX3   RFNG   RNF213   RPTOR   SECTM1   SGSH   SIRT7   SLC16A3   SLC25A10   SLC26A11   SLC38A10   TBC1D16   TBCD   TEPSIN   TEX19   TIMP2   TMEM105   TSPAN10   USP36   UTS2R   WDR45B   ZNF750  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371776,552,611 - 81,041,938CLINVAR
Cytogenetic Map1717q25.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13798092
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE


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