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Variant : CV676922 (GRCh37/hg19 1p34.1(chr1:46057301-46552564)x3) Homo sapiens

Symbol: CV676922
Name: GRCh37/hg19 1p34.1(chr1:46057301-46552564)x3
Condition: not provided [RCV000850025]
Clinical Significance: uncertain significance
Last Evaluated: 06/30/2017
Review Status: no assertion criteria provided
Related Genes: CCDC17   GPBP1L1   IPP   MAST2   NASP   PIK3R3   TMEM69  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37146,057,301 - 46,552,564CLINVAR
Cytogenetic Map11p34.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14981502
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


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