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Variant : CV555062 (GRCh37/hg19 11q24.2-25(chr11:127690585-132404117)x1) Homo sapiens

Symbol: CV555062
Name: GRCh37/hg19 11q24.2-25(chr11:127690585-132404117)x1
Condition: not provided [RCV000683367]
Clinical Significance: pathogenic
Last Evaluated: 05/04/2018
Review Status: no assertion criteria provided
Related Genes: ADAMTS15   ADAMTS8   APLP2   ARHGAP32   BARX2   C11orf45   ETS1   FLI1   KCNJ1   KCNJ5   LINC02873   NFRKB   NTM   OPCML   PRDM10   SNX19   ST14   TMEM45B   TP53AIP1   ZBTB44  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711127,690,585 - 132,404,117CLINVAR
Cytogenetic Map1111q24.2-25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13796520
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.