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Variant : CV605431 (GRCh37/hg19 13q21.1-31.3(chr13:57058434-94684615)x1) Homo sapiens

Symbol: CV605431
Name: GRCh37/hg19 13q21.1-31.3(chr13:57058434-94684615)x1
Condition: not provided [RCV000750731]
Clinical Significance: pathogenic
Last Evaluated: 09/20/2011
Review Status: no assertion criteria provided
Related Genes: ACOD1   ATXN8OS   BORA   CLN5   COMMD6   DACH1   DIAPH3   DIS3   EDNRB   FBXL3   GPC5   GPC6   KCTD12   KLF12   KLF5   KLHL1   LINC00402   LMO7   LMO7DN   MIR17   MIR17HG   MIR18A   MIR19A   MIR19B1   MIR20A   MIR4500HG   MIR92A1   MYCBP2   MZT1   NDFIP2   OBI1   PCDH17   PCDH20   PCDH9   PIBF1   POU4F1   PRR20A   PRR20B   PRR20C   PRR20D   PRR20E   RBM26   SCEL   SLAIN1   SLITRK1   SLITRK5   SLITRK6   SPRY2   TBC1D4   TDRD3   UCHL3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371357,058,434 - 94,684,615CLINVAR
Cytogenetic Map1313q21.1-31.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366057
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.