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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6873844copy number variation1nstd229human GRCh38 chr9: 128,809,701-128,819,200 , GRCh37.p13 chr9: 131,571,980-131,581,479 TBC1D13, SPOUT1, 1 more genes
    nsv6871252copy number variation1nstd229human GRCh38 chr9: 128,817,378-128,824,479 , GRCh37.p13 chr9: 131,579,657-131,586,758 SPOUT1, ENDOG
    nsv6867069copy number variation1nstd229human GRCh38 chr9: 128,815,856-128,818,557 , GRCh37.p13 chr9: 131,578,135-131,580,836 SPOUT1, ENDOG
    nsv6860073copy number variation1nstd229human GRCh38 chr9: 128,817,343-128,818,156 , GRCh37.p13 chr9: 131,579,622-131,580,435 ENDOG, SPOUT1
    nsv6860019copy number variation1nstd229human GRCh38 chr9: 128,721,801-128,940,900 , GRCh37.p13 chr9: 131,484,080-131,703,179 ENDOG, SPOUT1, 8 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
    nsv6448999copy number variation1nstd223human GRCh38 chr9: 128,817,374-128,818,108 , GRCh37.p13 chr9: 131,579,653-131,580,387 ENDOG, SPOUT1
    nsv6448188copy number variation1nstd223human GRCh38 chr9: 128,817,601-128,819,800 , GRCh37.p13 chr9: 131,579,880-131,582,079 ENDOG, SPOUT1
    nsv6437346copy number variation1nstd223human GRCh38 chr9: 128,821,693-128,822,783 , GRCh37.p13 chr9: 131,583,972-131,585,062 SPOUT1, ENDOG
    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
    nsv6270206copy number variation1nstd214human GRCh38 chr9: 128,821,344-128,821,421 , GRCh37.p13 chr9: 131,583,623-131,583,700 SPOUT1, ENDOG
    nsv6269360copy number variation1nstd214human GRCh38 chr9: 128,821,354-128,821,431 , GRCh37.p13 chr9: 131,583,633-131,583,710 SPOUT1, ENDOG
    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
    nsv5910743copy number variation1nstd209human GRCh38 chr9: 128,817,374-128,818,107 , GRCh37.p13 chr9: 131,579,653-131,580,386 SPOUT1, ENDOG
    nsv5481537copy number variation1nstd206human GRCh38 chr9: 128,814,632-128,817,294 , GRCh37.p13 chr9: 131,576,911-131,579,573 ENDOG
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