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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912957copy number variation1nstd209human GRCh38 chr8: 30,677,201-30,677,576 , GRCh37.p13 chr8: 30,534,718-30,535,093 GSR
    nsv5490745copy number variation1nstd206human GRCh38 chr8: 30,677,484-30,678,918 , GRCh37.p13 chr8: 30,535,001-30,536,435 GSR
    nsv5479863copy number variation1nstd206human GRCh38 chr8: 30,677,201-30,677,567 , GRCh37.p13 chr8: 30,534,718-30,535,084 GSR
    nsv5475126copy number variation1nstd206human GRCh38 chr8: 30,725,314-30,726,523 , GRCh37.p13 chr8: 30,582,831-30,584,040 GSR
    nsv5363979translocation1nstd200human GRCh38 chr8: 30,692,434-30,692,434 , GRCh38 chr8: 30,692,608-30,692,608 , GRCh37.p13 chr8: 30,549,951-30,549,951 , GRCh37.p13 chr8: 30,550,125-30,550,125 GSR
    nsv5344582translocation1nstd200human GRCh37 chr8: 30,547,968-30,547,968 , GRCh37 chr8: 30,438,466-30,438,466 , GRCh38.p12 chr8: 30,580,949-30,580,949 , GRCh38.p12 chr8: 30,690,451-30,690,451 GTF2E2, GSR
    nsv5336277translocation1nstd200human GRCh37 chr8: 30,550,125-30,550,125 , GRCh37 chr8: 30,549,951-30,549,951 , GRCh38.p12 chr8: 30,692,608-30,692,608 , GRCh38.p12 chr8: 30,692,434-30,692,434 GSR
    nsv5301473copy number variation1nstd204human GRCh38.p13 chr8: 30,572,869-30,699,580 , GRCh37.p13 chr8: 30,430,386-30,557,097 , RNU5A-3P, 3 more genes
    nsv5257133copy number variation1nstd204human GRCh38.p13 chr8: 30,618,301-30,699,600 , GRCh37.p13 chr8: 30,475,818-30,557,117 GTF2E2, RNU5A-3P, 2 more genes
    nsv5257028copy number variation1nstd204human GRCh38.p13 chr8: 30,690,658-30,699,580 , GRCh37.p13 chr8: 30,548,175-30,557,097 GSR
    nsv5255579copy number variation1nstd204human GRCh38.p13 chr8: 30,687,463-30,690,357 , GRCh37.p13 chr8: 30,544,980-30,547,874 GSR
    nsv5252167copy number variation1nstd204human GRCh38.p13 chr8: 30,656,309-30,685,637 , GRCh37.p13 chr8: 30,513,826-30,543,154 GTF2E2, GSR
    nsv5246172copy number variation1nstd204human GRCh38.p13 chr8: 30,686,363-30,688,398 , GRCh37.p13 chr8: 30,543,880-30,545,915 GSR
    nsv5244972copy number variation1nstd204human GRCh38.p13 chr8: 30,694,058-30,697,057 , GRCh37.p13 chr8: 30,551,575-30,554,574 GSR
    nsv5240430copy number variation1nstd204human GRCh38.p13 chr8: 30,695,558-30,699,257 , GRCh37.p13 chr8: 30,553,075-30,556,774 GSR
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5117744mobile element insertion1nstd203human GRCh38 chr8: 30,711,437-30,711,454 , GRCh37.p13 chr8: 30,568,954-30,568,971 GSR
    nsv5111317mobile element insertion1nstd203human GRCh38 chr8: 30,695,064-30,695,078 , GRCh37.p13 chr8: 30,552,581-30,552,595 GSR
    nsv4959969copy number variation1nstd200human GRCh38 chr8: 30,700,564-30,702,132 , GRCh37.p13 chr8: 30,558,081-30,559,649 GSR
    nsv4954307copy number variation1nstd200human GRCh38 chr8: 30,572,879-30,699,571 , GRCh37.p13 chr8: 30,430,396-30,557,088 , SMIM18, 3 more genes
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