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Variant : CV157595 (GRCh38/hg38 2q37.2-37.3(chr2:235028429-242066108)x1) Homo sapiens

Symbol: CV157595
Name: GRCh38/hg38 2q37.2-37.3(chr2:235028429-242066108)x1
Condition: See cases [RCV000136968]
Clinical Significance: pathogenic
Last Evaluated: 09/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACKR3   AGAP1   AGAP1-IT1   AGXT   ANKMY1   ANO7   AQP12A   AQP12B   ASB1   ASB18   ATG4B   BOK   BOK-AS1   CAPN10   CAPN10-DT   COL6A3   COPS8   COPS9   CROCC2   D2HGDH   DTYMK   DUSP28   ERFE   ESPNL   FARP2   GAL3ST2   GBX2   GPC1   GPR35   HDAC4   HDAC4-AS1   HDLBP   HES6   ILKAP   ING5   IQCA1   KIF1A   KLHL30   LINC01107   LINC01237   LINC01238   LINC01880   LINC01937   LINC01940   LINC02610   LOC285097   LRRFIP1   MAB21L4   MIR149   MIR2467   MIR3133   MIR4269   MIR4440   MIR4441   MIR4786   MIR6811   MLPH   MTERF4   NDUFA10   NEU4   OR6B2   OR6B3   OTOS   PASK   PDCD1   PER2   PPP1R7   PRLH   PRR21   RAB17   RAMP1   RBM44   RNPEPL1   RTP5   SCLY   SEPTIN2   SH3BP4   SNED1   STK25   THAP4   TNRC17   TRAF3IP1   TWIST2   UBE2F   UBE2F-SCLY  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_235028429)_(242066108_?)del
NC_000002.11:g.(?_235937073)_(243008259_?)del
NC_000002.10:g.(?_235601812)_(242656932_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382235,028,429 - 242,066,108CLINVAR
GRCh372235,937,073 - 243,008,259CLINVAR
Build 362235,601,812 - 242,656,932CLINVAR
Cytogenetic Map22q37.2-37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484529
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.