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Variant : CV162877 (GRCh38/hg38 2q37.3(chr2:241565848-242110155)x1) Homo sapiens

Symbol: CV162877
Name: GRCh38/hg38 2q37.3(chr2:241565848-242110155)x1
Condition: See cases [RCV000141625]
Clinical Significance: uncertain significance
Last Evaluated: 06/25/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ATG4B   BOK   D2HGDH   DTYMK   FAM240C   GAL3ST2   ING5   LINC01237   LINC01238   LINC01880   LINC01881   LOC285097   NEU4   PDCD1   RTP5   THAP4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_241565848)_(242110155_?)del
NC_000002.11:g.(?_242505263)_(243052306_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382241,565,848 - 242,110,155CLINVAR
GRCh372242,505,263 - 243,052,306CLINVAR
Build 362242,153,936 - 242,700,979CLINVAR
Cytogenetic Map22q37.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489150
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-12
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.