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Variant : CV154573 (GRCh38/hg38 2p11.2(chr2:89033009-90225016)x1) Homo sapiens

Symbol: CV154573
Name: GRCh38/hg38 2p11.2(chr2:89033009-90225016)x1
Condition: See cases [RCV000134226]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGK   IGKV1-12   IGKV1-13   IGKV1-16   IGKV1-17   IGKV1-27   IGKV1-33   IGKV1-37   IGKV1-39   IGKV1D-12   IGKV1D-13   IGKV1D-16   IGKV1D-17   IGKV1D-33   IGKV1D-37   IGKV1D-39   IGKV1D-42   IGKV1D-43   IGKV1D-8   IGKV2-24   IGKV2-28   IGKV2-30   IGKV2-40   IGKV2D-24   IGKV2D-28   IGKV2D-29   IGKV2D-30   IGKV2D-40   IGKV3-15   IGKV3-20   IGKV3D-11   IGKV3D-15   IGKV3D-20   IGKV6-21   IGKV6D-21   IGKV6D-41  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_89033009)_(90225016_?)del
NC_000002.11:g.(?_89332506)_(90263882_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38289,033,009 - 90,225,016CLINVAR
GRCh37289,332,506 - 90,263,882CLINVAR
Build 36289,113,621 - 89,901,187CLINVAR
Cytogenetic Map22p11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481806
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.