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Variant : CV593704 (GRCh37/hg19 16p13.3(chr16:2142976-2311160)x3) Homo sapiens

Symbol: CV593704
Name: GRCh37/hg19 16p13.3(chr16:2142976-2311160)x3
Condition: not provided [RCV000739004]
Clinical Significance: benign
Last Evaluated: 03/09/2013
Review Status: no assertion criteria provided
Related Genes: BRICD5   CASKIN1   DNASE1L2   E4F1   ECI1   MLST8   PGP   PKD1   RAB26   RNPS1   TRAF7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37162,142,976 - 2,311,160CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14354381
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.