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Variant : CV673832 (GRCh37/hg19 12p13.33(chr12:224051-310571)x1) Homo sapiens

Symbol: CV673832
Name: GRCh37/hg19 12p13.33(chr12:224051-310571)x1
Condition: not provided [RCV000846948]
Clinical Significance: uncertain significance
Last Evaluated: 06/21/2018
Review Status: no assertion criteria provided
Related Genes: IQSEC3   SLC6A12  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3712224,051 - 310,571CLINVAR
Cytogenetic Map1212p13.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977519
Created: 2019-10-08
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.