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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 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
    nsv7069423inversion1nstd229human GRCh38 chr9: 129,538,596-129,734,493 , GRCh37.p13 chr9: 132,300,875-132,496,772 ASB6, C9orf50, 4 more genes
    nsv7068973inversion1nstd229human GRCh38 chr9: 129,470,380-129,658,423 , GRCh37.p13 chr9: 132,232,659-132,420,702 LINC00963, NTMT1, 3 more genes
    nsv7062544inversion1nstd229human GRCh38 chr9: 129,540,381-129,734,488 , GRCh37.p13 chr9: 132,302,660-132,496,767 LOC105376292, NTMT1, 4 more genes
    nsv7059203inversion1nstd229human GRCh38 chr9: 129,607,019-129,820,587 , GRCh37.p13 chr9: 132,369,298-132,582,866 PRRX2, PRRX2-AS1, 7 more genes
    nsv6873399copy number variation1nstd229human GRCh38 chr9: 129,635,201-129,638,700 , GRCh37.p13 chr9: 132,397,480-132,400,979 ASB6, NTMT1
    nsv6868828copy number variation1nstd229human GRCh38 chr9: 129,550,101-129,665,900 , GRCh37.p13 chr9: 132,312,380-132,428,179 PRRX2, LOC105376292, 3 more genes
    nsv6868595copy number variation1nstd229human GRCh38 chr9: 129,339,601-129,648,300 , GRCh37.p13 chr9: 132,101,880-132,410,579 LOC105376291, C9orf50, 7 more genes
    nsv6573040inversion1nstd223human GRCh38 chr9: 129,607,011-129,820,589 , GRCh37.p13 chr9: 132,369,290-132,582,868 TOR1A, PTGES, 7 more genes
    nsv6570274inversion1nstd223human GRCh38 chr9: 129,538,594-129,734,493 , GRCh37.p13 chr9: 132,300,873-132,496,772 NTMT1, PRRX2, 4 more genes
    nsv6447256copy number variation1nstd223human GRCh38 chr9: 129,483,666-129,733,968 , GRCh37.p13 chr9: 132,245,945-132,496,247 LINC00963, PRRX2, 5 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
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
    nsv6008653copy number variation1nstd212human GRCh38 chr9: 129,642,476-129,643,121 , GRCh37.p13 chr9: 132,404,755-132,405,400 ASB6
    nsv5912574copy number variation1nstd209human GRCh38 chr9: 129,636,326-129,636,547 , GRCh37.p13 chr9: 132,398,605-132,398,826 NTMT1, ASB6
    nsv5909290copy number variation1nstd209human GRCh38 chr9: 129,642,476-129,643,120 , GRCh37.p13 chr9: 132,404,755-132,405,399 ASB6
    nsv5480308copy number variation1nstd206human GRCh38 chr9: 129,642,484-129,643,121 , GRCh37.p13 chr9: 132,404,763-132,405,400 ASB6
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