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Variant : CV248208 (GRCh37/hg19 1p35.3(chr1:28292253-28969539)x3) Homo sapiens

Symbol: CV248208
Name: GRCh37/hg19 1p35.3(chr1:28292253-28969539)x3
Condition: See cases [RCV000240431]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ATP5IF1   DNAJC8   EYA3   MED18   PHACTR4   PTAFR   RAB42   RCC1   SESN2   SNHG3   SNORA73A   TAF12   TRNAU1AP   XKR8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37128,292,253 - 28,969,539CLINVAR
Cytogenetic Map11p35.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541828
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-02-04
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.