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Variant : CV673459 (GRCh37/hg19 13q14.2-21.2(chr13:49586017-61311845)x1) Homo sapiens

Symbol: CV673459
Name: GRCh37/hg19 13q14.2-21.2(chr13:49586017-61311845)x1
Condition: not provided [RCV000846575]
Clinical Significance: uncertain significance
Last Evaluated: 03/01/2018
Review Status: no assertion criteria provided
Related Genes: ALG11   ARL11   ATP7B   CAB39L   CCDC70   CDADC1   CKAP2   CNMD   DHRS12   DIAPH3   DLEU1   DLEU2   DLEU7   EBPL   FAM124A   FNDC3A   HNRNPA1L2   INTS6   KCNRG   KPNA3   LINC00558   MIR15A   MIR16-1   MLNR   NEK3   NEK5   OLFM4   PCDH17   PCDH8   PHF11   PRR20A   PRR20B   PRR20C   PRR20D   PRR20E   RCBTB1   RNASEH2B   SERPINE3   SETDB2   SPRYD7   SUGT1   TDRD3   THSD1   TRIM13   UTP14C   VPS36   WDFY2  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371349,586,017 - 61,311,845CLINVAR
Cytogenetic Map1313q14.2-21.2CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14977142
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


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