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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146254copy number variation1nstd232human GRCh37.p13 chr9: 131,745,657-131,745,749 , GRCh38.p12 chr9: 128,983,378-128,983,470 NUP188
    nsv7138928insertion1nstd232human GRCh37.p13 chr9: 131,749,149-131,749,149 , GRCh38.p12 chr9: 128,986,870-128,986,870 NUP188
    nsv7137983copy number variation1nstd232human GRCh38.p12 chr9: 129,005,219-129,005,299 , GRCh37.p13 chr9: 131,767,498-131,767,578 NUP188, SH3GLB2, 1 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7070239inversion1nstd229human GRCh38 chr9: 128,869,438-129,153,886 , GRCh37.p13 chr9: 131,631,717-131,916,165 DOLK, PTPA, 10 more genes
    nsv6870299copy number variation1nstd229human GRCh38 chr9: 128,946,856-128,946,899 , GRCh37.p13 chr9: 131,709,135-131,709,178 NUP188, DOLK
    nsv6633345copy number variation1nstd224human GRCh37 chr9: 131,696,074-131,708,883 , GRCh38.p12 chr9: 128,933,795-128,946,604 PHYHD1, NUP188, 1 more genes
    nsv6573658inversion1nstd223human GRCh38 chr9: 128,961,458-128,961,945 , GRCh37.p13 chr9: 131,723,737-131,724,224 NUP188
    nsv6567544inversion1nstd223human GRCh38 chr9: 128,959,585-128,961,061 , GRCh37.p13 chr9: 131,721,864-131,723,340 NUP188
    nsv6564525inversion1nstd223human GRCh38 chr9: 128,952,036-128,952,170 , GRCh37.p13 chr9: 131,714,315-131,714,449 NUP188
    nsv6562382inversion1nstd223human GRCh38 chr9: 129,000,347-129,000,781 , GRCh37.p13 chr9: 131,762,626-131,763,060 NUP188, LOC101929314
    nsv6560845inversion1nstd223human GRCh38 chr9: 128,976,972-128,977,344 , GRCh37.p13 chr9: 131,739,251-131,739,623 NUP188
    nsv6448863copy number variation1nstd223human GRCh38 chr9: 128,962,528-128,965,878 , GRCh37.p13 chr9: 131,724,807-131,728,157 NUP188
    nsv6445158copy number variation1nstd223human GRCh38 chr9: 128,959,574-128,960,634 , GRCh37.p13 chr9: 131,721,853-131,722,913 NUP188
    nsv6437267copy number variation1nstd223human GRCh38 chr9: 128,935,351-128,951,038 , GRCh37.p13 chr9: 131,697,630-131,713,317 DOLK, PHYHD1, 1 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
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6240253mobile element insertion1nstd215human GRCh38 chr9: 128,958,701-128,958,701 , GRCh37.p13 chr9: 131,720,980-131,720,980 NUP188
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