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Variant : CV158595 (GRCh38/hg38 3q26.33(chr3:182192428-182657097)x1) Homo sapiens

Symbol: CV158595
Name: GRCh38/hg38 3q26.33(chr3:182192428-182657097)x1
Condition: See cases [RCV000137909]
Clinical Significance: uncertain significance
Last Evaluated: 10/26/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC01994   LINC01995   LINC02031  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_182192428)_(182657097_?)del
NC_000003.11:g.(?_181910216)_(182374885_?)del
NC_000003.10:g.(?_183392910)_(183857579_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383182,192,428 - 182,657,097CLINVAR
GRCh373181,910,216 - 182,374,885CLINVAR
Build 363183,392,910 - 183,857,579CLINVAR
Cytogenetic Map33q26.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485460
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.