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Variant : CV672762 (GRCh37/hg19 16p13.3(chr16:2070917-2592737)x3) Homo sapiens

Symbol: CV672762
Name: GRCh37/hg19 16p13.3(chr16:2070917-2592737)x3
Condition: not provided [RCV000845878]
Clinical Significance: uncertain significance
Last Evaluated: 08/11/2017
Review Status: no assertion criteria provided
Related Genes: ABCA3   AMDHD2   ATP6V0C   BRICD5   CASKIN1   CCNF   CEMP1   DNASE1L2   E4F1   ECI1   MIR1225   MLST8   NTHL1   NTN3   PDPK1   PGP   PKD1   RAB26   RNPS1   SLC9A3R2   TBC1D24   TEDC2   TRAF7   TSC2  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37162,070,917 - 2,592,737CLINVAR
Cytogenetic Map1616p13.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14976357
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.