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Variant : CV555629 (GRCh37/hg19 17q21.2(chr17:39043189-39492499)x1) Homo sapiens

Symbol: CV555629
Name: GRCh37/hg19 17q21.2(chr17:39043189-39492499)x1
Condition: not provided [RCV000683934]
Clinical Significance: likely benign
Last Evaluated: 11/03/2017
Review Status: no assertion criteria provided
Related Genes: KRT23   KRT39   KRT40   KRTAP1-1   KRTAP1-3   KRTAP1-4   KRTAP1-5   KRTAP16-1   KRTAP17-1   KRTAP2-1   KRTAP2-2   KRTAP2-3   KRTAP2-4   KRTAP3-1   KRTAP3-2   KRTAP3-3   KRTAP4-1   KRTAP4-11   KRTAP4-12   KRTAP4-2   KRTAP4-3   KRTAP4-4   KRTAP4-5   KRTAP4-6   KRTAP4-7   KRTAP4-8   KRTAP4-9   KRTAP9-1   KRTAP9-2   KRTAP9-3   KRTAP9-4   KRTAP9-6   KRTAP9-7   KRTAP9-8   KRTAP9-9  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371739,043,189 - 39,492,499CLINVAR
Cytogenetic Map1717q21.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798000
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-09-10
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.