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Variant : CV434735 (GRCh37/hg19 8p22-12(chr8:16992973-32612724)x1) Homo sapiens

Symbol: CV434735
Name: GRCh37/hg19 8p22-12(chr8:16992973-32612724)x1
Condition: not provided [RCV000509389]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: ADAM28   ADAM7   ADAMDEC1   ADRA1A   ASAH1   ATP6V1B2   BIN3   BMP1   BNIP3L   C8orf58   CCAR2   CCDC25   CDCA2   CHMP7   CHRNA2   CLU   CNOT7   CSGALNACT1   DCTN6   DMTN   DOCK5   DOK2   DPYSL2   DUSP4   EBF2   EGR3   ELP3   ENTPD4   EPHX2   ESCO2   EXTL3   FAM160B2   FBXO16   FGF17   FGL1   FZD3   GFRA2   GNRH1   GSR   GTF2E2   HMBOX1   HR   INTS10   INTS9   KCTD9   KIF13B   LEPROTL1   LGI3   LOXL2   LPL   LZTS1   MBOAT4   MIR320A   MTMR7   MTUS1   NAT1   NAT2   NEFL   NEFM   NKX2-6   NKX3-1   NPM2   NRG1   NUDT18   NUGGC   PBK   PCM1   PDGFRL   PDLIM2   PEBP4   PHYHIP   PIWIL2   PNMA2   PNOC   POLR3D   PPP2CB   PPP2R2A   PPP3CC   PSD3   PTK2B   PURG   R3HCC1   RBPMS   REEP4   RHOBTB2   SARAF   SCARA3   SCARA5   SFTPC   SH2D4A   SLC18A1   SLC25A37   SLC39A14   SLC7A2   SMIM18   SORBS3   STC1   STMN4   TEX15   TNFRSF10A   TNFRSF10B   TNFRSF10C   TNFRSF10D   TRIM35   UBXN8   VPS37A   WRN   XPO7   ZDHHC2   ZNF395  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: phenotyping only
Position
Human AssemblyChrPosition (strand)Source
GRCh37816,992,973 - 32,612,724CLINVAR
Cytogenetic Map88p22-12CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13442599
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
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.