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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915293copy number variation1nstd209human GRCh38 chr8: 47,200,995-47,201,100 , GRCh37.p13 chr8: 48,112,618-48,112,723 IGLV8OR8-1
    nsv5354042translocation1nstd200human GRCh38 chr15: 48,339,835-48,339,835 , GRCh38 chr8: 47,201,156-47,201,156 , GRCh37.p13 chr8: 48,112,779-48,112,779 , GRCh37.p13 chr15: 48,632,032-48,632,032 IGLV8OR8-1, DUT
    nsv5335436translocation1nstd200human GRCh37 chr15: 48,632,032-48,632,032 , GRCh37 chr8: 48,112,779-48,112,779 , GRCh38.p12 chr15: 48,339,835-48,339,835 , GRCh38.p12 chr8: 47,201,156-47,201,156 IGLV8OR8-1, DUT
    nsv4952071copy number variation1nstd200human GRCh38 chr8: 47,083,070-47,201,303 , GRCh37.p13 chr8: 47,994,693-48,112,926 LOC105375815, RNU6-819P, 8 more genes
    nsv4825802copy number variation1nstd200human GRCh37 chr8: 48,112,618-48,112,726 , GRCh38.p12 chr8: 47,200,995-47,201,103 IGLV8OR8-1
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4728835copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,089,553-48,222,687 , GRCh38.p12 chr8: 47,177,930-47,276,395 ATP6V1G1P2, IGLV8OR8-1, 2 more genes
    nsv4701721copy number variation1nstd195human GRCh37 chr8: 48,088,951-48,130,501 , GRCh38.p12 chr8: 47,177,328-47,218,876 ATP6V1G1P2, LOC100287846, 1 more genes
    nsv4675356copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,058,961-48,260,865 , GRCh38.p12 chr8: 47,147,338-47,348,298 SPIDR, ATP6V1G1P2, 4 more genes
    nsv4611972copy number variation1nstd183human GRCh37 chr8: 46,847,534-48,392,708 , GRCh38.p12 chr8: 45,935,912-47,480,146 LOC105375816, NDUFA5P12, 29 more genes
    nsv4525737copy number variation1nstd166human GRCh37.p13 chr8: 47,938,899-48,259,000 , GRCh38.p12 chr8: 47,027,276-47,346,433 LOC105375817, RPL10AP2, 10 more genes
    nsv4457018copy number variation1nstd102humanUncertain significance GRCh37 chr8: 46,851,293-48,277,752 , GRCh38.p12 chr8: 45,939,671-47,365,184 LOC100287846, LOC105375812, 29 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4154832copy number variation1nstd166human GRCh37.p13 chr8: 48,114,983-48,121,494 , GRCh38.p12 chr8: 47,203,360-47,209,871 IGLV8OR8-1
    nsv3961443copy number variation1nstd168human GRCh38 chr8: 47,128,440-47,203,153 , GRCh37.p13 chr8: 48,040,063-48,114,776 RPL10AP2, ATP6V1G1P2, 5 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
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