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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142594insertion1nstd232human GRCh37.p13 chr9: 129,576,552-129,576,552 , GRCh38.p12 chr9: 126,814,273-126,814,273 ZBTB43
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7062721inversion1nstd229human GRCh38 chr9: 126,817,235-126,817,609 , GRCh37.p13 chr9: 129,579,514-129,579,888 ZBTB43
    nsv6874242copy number variation1nstd229human GRCh38 chr9: 126,815,758-126,821,000 , GRCh37.p13 chr9: 129,578,037-129,583,279 ZBTB43
    nsv6871622copy number variation1nstd229human GRCh38 chr9: 126,811,202-126,811,235 , GRCh37.p13 chr9: 129,573,481-129,573,514 ZBTB43
    nsv6866345copy number variation1nstd229human GRCh38 chr9: 126,814,287-126,817,606 , GRCh37.p13 chr9: 129,576,566-129,579,885 ZBTB43
    nsv6865289copy number variation1nstd229human GRCh38 chr9: 126,799,101-126,804,600 , GRCh37.p13 chr9: 129,561,380-129,566,879 ZBTB43
    nsv6863915copy number variation1nstd229human GRCh38 chr9: 126,812,165-126,815,097 , GRCh37.p13 chr9: 129,574,444-129,577,376 ZBTB43
    nsv6858908copy number variation1nstd229human GRCh38 chr9: 126,789,822-126,813,416 , GRCh37.p13 chr9: 129,552,101-129,575,695 ZBTB43
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634298copy number variation1nstd102humanPathogenic GRCh38 chr9: 126,507,040-126,804,072 , GRCh37.p13 chr9: 129,269,319-129,566,351 LMX1B, ZBTB43, 4 more genes
    nsv6571873inversion1nstd223human GRCh38 chr9: 126,817,235-126,817,609 , GRCh37.p13 chr9: 129,579,514-129,579,888 ZBTB43
    nsv6568657inversion1nstd223human GRCh38 chr9: 126,821,267-126,822,147 , GRCh37.p13 chr9: 129,583,546-129,584,426 ZBTB43
    nsv6561356inversion1nstd223human GRCh38 chr9: 126,810,520-126,811,170 , GRCh37.p13 chr9: 129,572,799-129,573,449 ZBTB43
    nsv6558470inversion1nstd223human GRCh38 chr9: 126,810,142-126,811,010 , GRCh37.p13 chr9: 129,572,421-129,573,289 ZBTB43
    nsv6441096copy number variation1nstd223human GRCh38 chr9: 126,746,401-126,832,100 , GRCh37.p13 chr9: 129,508,680-129,594,379 ZBTB43
    nsv6438803copy number variation1nstd223human GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679 MIR199B, FPGS, 72 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
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