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Items: 1 to 20 of 220

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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
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6452384copy number variation1nstd223human GRCh38 chr9: 128,698,901-128,708,000 , GRCh37.p13 chr9: 131,461,180-131,470,279 PKN3, RN7SL560P
    nsv6447933copy number variation1nstd223human GRCh38 chr9: 128,699,201-128,710,575 , GRCh37.p13 chr9: 131,461,480-131,472,854 PKN3, RN7SL560P
    nsv6436848copy number variation1nstd223human GRCh38 chr9: 128,712,196-128,717,319 , GRCh37.p13 chr9: 131,474,475-131,479,598 PKN3
    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
    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
    nsv6089071insertion1nstd212human GRCh38 chr9: 128,706,448-128,706,448 , GRCh37.p13 chr9: 131,468,727-131,468,727 PKN3
    nsv6018650copy number variation1nstd212human GRCh38 chr9: 128,710,004-128,710,102 , GRCh37.p13 chr9: 131,472,283-131,472,381 RN7SL560P, PKN3
    nsv5962890insertion1nstd209human GRCh38 chr9: 128,717,117-128,717,117 , GRCh37.p13 chr9: 131,479,396-131,479,396 PKN3
    nsv5962534insertion1nstd209human GRCh38 chr9: 128,701,941-128,701,941 , GRCh37.p13 chr9: 131,464,220-131,464,220 PKN3
    nsv5923901copy number variation1nstd209human GRCh38 chr9: 128,706,379-128,706,471 , GRCh37.p13 chr9: 131,468,658-131,468,750 PKN3
    nsv5853721copy number variation1nstd209human GRCh38 chr9: 128,714,431-128,715,630 , GRCh37.p13 chr9: 131,476,710-131,477,909 PKN3
    nsv5631665insertion1nstd207human GRCh38 chr9: 128,706,379-128,706,379 , GRCh37.p13 chr9: 131,468,658-131,468,658 PKN3
    nsv5488178copy number variation1nstd206human GRCh38 chr9: 128,699,179-128,700,916 , GRCh37.p13 chr9: 131,461,458-131,463,195 PKN3
    nsv5251878copy number variation1nstd204human GRCh38.p13 chr9: 128,649,801-128,795,400 , GRCh37.p13 chr9: 131,412,080-131,557,679 , DYNC2I2, 9 more genes
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