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Variant : CV434742 (GRCh37/hg19 13q14.3(chr13:51786657-54834098)x1) Homo sapiens

Symbol: CV434742
Name: GRCh37/hg19 13q14.3(chr13:51786657-54834098)x1
Condition: not provided [RCV000509218]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: ALG11   ATP7B   CCDC70   CKAP2   CNMD   DHRS12   FAM124A   HNRNPA1L2   INTS6   LINC00558   NEK3   NEK5   OLFM4   PCDH8   SERPINE3   SUGT1   THSD1   UTP14C   VPS36   WDFY2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: phenotyping only
Position
Human AssemblyChrPosition (strand)Source
GRCh371351,786,657 - 54,834,098CLINVAR
Cytogenetic Map1313q14.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13442575
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-21
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.