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Variant : CV164985 (GRCh38/hg38 9p21.1(chr9:30071864-31270467)x1) Homo sapiens

Symbol: CV164985
Name: GRCh38/hg38 9p21.1(chr9:30071864-31270467)x1
Condition: See cases [RCV000143298]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 09/27/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC01242  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_30071864)_(31270467_?)del
NC_000009.11:g.(?_30071862)_(31270465_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38930,071,864 - 31,270,467CLINVAR
GRCh37930,071,862 - 31,270,465CLINVAR
Build 36930,061,862 - 31,260,465CLINVAR
Cytogenetic Map99p21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490896
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.