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Variant : CV383610 (GRCh37/hg19 1p32.3(chr1:55121535-55381546)x3) Homo sapiens

Symbol: CV383610
Name: GRCh37/hg19 1p32.3(chr1:55121535-55381546)x3
Condition: See cases [RCV000448663]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: DHCR24   LEXM   MROH7   PARS2   TTC22   TTC4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.10:g.(?_55121535)_(55381546_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh37155,121,535 - 55,381,546CLINVAR
Cytogenetic Map11p32.3CLINVAR




Additional Information

 
CRRD Object Information
CRRD ID: 12853367
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2017-10-03
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.