Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV157594 (GRCh38/hg38 2q36.3-37.2(chr2:228014149-234976424)x3) Homo sapiens

Symbol: CV157594
Name: GRCh38/hg38 2q36.3-37.2(chr2:228014149-234976424)x3
Condition: See cases [RCV000136967]
Clinical Significance: pathogenic
Last Evaluated: 09/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ALPG   ALPI   ALPP   ARL4C   ARMC9   ATG16L1   B3GNT7   C2orf72   CAB39   CHRND   CHRNG   COPS7B   DGKD   DIS3L2   DNAJB3   DNER   ECEL1   EFHD1   EIF4E2   FBXO36   GCSIR   GIGYF2   GPR55   HJURP   HTR2B   INPP5D   ITM2C   KCNJ13   LINC00471   LINC01173   LINC01807   LINC01891   LINC01907   MIR1244-1   MIR1471   MIR4777   MIR5001   MIR562   MROH2A   NCL   NEU2   NGEF   NMUR1   NPPC   PDE6D   PID1   PRSS56   PSMD1   PTMA   SAG   SCARNA5   SCARNA6   SH3BP4   SLC16A14   SNORA75   SNORC   SNORD20   SNORD82   SP100   SP110   SP140   SP140L   SPATA3   SPATA3-AS1   SPHKAP   SPP2   TEX44   TIGD1   TRIP12   TRPM8   UGT1A   UGT1A1   UGT1A10   UGT1A3   UGT1A4   UGT1A5   UGT1A6   UGT1A7   UGT1A8   UGT1A9   USP40  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_228014149)_(234976424_?)dup
NC_000002.11:g.(?_228878865)_(235885068_?)dup
NC_000002.10:g.(?_228587109)_(235549807_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382228,014,149 - 234,976,424CLINVAR
GRCh372228,878,865 - 235,885,068CLINVAR
Build 362228,587,109 - 235,549,807CLINVAR
Cytogenetic Map22q36.3-37.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484528
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
Status: ACTIVE



NHLBI Logo

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