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Variant : CV672949 (GRCh37/hg19 9p24.3(chr9:203861-1670196)x3) Homo sapiens

Symbol: CV672949
Name: GRCh37/hg19 9p24.3(chr9:203861-1670196)x3
Condition: not provided [RCV000846065]
Clinical Significance: uncertain significance
Last Evaluated: 09/29/2017
Review Status: no assertion criteria provided
Related Genes: DMRT1   DMRT2   DMRT3   DOCK8   DOCK8-AS1   KANK1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379203,861 - 1,670,196CLINVAR
Cytogenetic Map99p24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976609
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.