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Variant : CV437108 (GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3) Homo sapiens

Symbol: CV437108
Name: GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3
Condition: See cases [RCV000510919]
Clinical Significance: pathogenic
Last Evaluated: 10/21/2014
Review Status: no assertion criteria provided
Related Genes: AANAT   AATK   ACOX1   ACTG1   AFMID   ALYREF   ANAPC11   ARHGDIA   ARL16   ASPSCR1   B3GNTL1   BAHCC1   BAIAP2   BIRC5   C17orf99   C1QTNF1   CANT1   CARD14   CBX2   CBX4   CBX8   CCDC137   CCDC40   CCDC57   CD7   CDK3   CENPX   CEP131   CHMP6   CSNK1D   CYBC1   CYGB   CYTH1   DCXR   DNAH17   DUS1L   EIF4A3   ENDOV   ENGASE   ENPP7   EVPL   EXOC7   FAAP100   FASN   FN3K   FN3KRP   FOXJ1   FOXK2   FSCN2   GAA   GALR2   GCGR   GPS1   HEXD   HEXD-IT1   HGS   JMJD6   LGALS3BP   LRRC45   MAFG   MCRIP1   METRNL   METTL23   MFSD11   MGAT5B   MIR338   MRPL12   MXRA7   MYADML2   NARF   NDUFAF8   NOTUM   NPB   NPLOC4   NPTX1   OGFOD3   OXLD1   P4HB   PCYT2   PDE6G   PGS1   PPP1R27   PRCD   PRPSAP1   PYCR1   QRICH2   RAB40B   RAC3   RBFOX3   RFNG   RHBDF2   RNF157   RNF213   RPTOR   SEC14L1   SECTM1   SEPTIN9   SGSH   SIRT7   SLC16A3   SLC25A10   SLC26A11   SLC38A10   SOCS3   SPHK1   SRP68   SRSF2   ST6GALNAC1   ST6GALNAC2   SYNGR2   TBC1D16   TBCD   TEN1   TEPSIN   TEX19   TIMP2   TK1   TMC6   TMC8   TMEM105   TMEM235   TNRC6C   TSPAN10   UBALD2   UBE2O   USP36   UTS2R   WDR45B   ZACN   ZNF750  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371773,951,701 - 81,041,938CLINVAR
Cytogenetic Map1717q25.1-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443896
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-17
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.