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Variant : CV556143 (GRCh37/hg19 Yp11.2(chrY:6138309-9168128)x0) Homo sapiens

Symbol: CV556143
Name: GRCh37/hg19 Yp11.2(chrY:6138309-9168128)x0
Condition: not provided [RCV000684434]
Clinical Significance: likely benign
Last Evaluated: 06/27/2017
Review Status: no assertion criteria provided
Related Genes: AMELY   TBL1Y   TTTY11   TTTY12   TTTY13B   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY20   TTTY21B   TTTY2B   TTTY7   TTTY8B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37Y6,138,309 - 9,168,128CLINVAR
Cytogenetic MapYYp11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798670
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-19
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.