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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7068792inversion1nstd229human GRCh38 chr9: 128,060,909-128,060,993 , GRCh37.p13 chr9: 130,823,188-130,823,272 NAIF1
    nsv6872162copy number variation1nstd229human GRCh38 chr9: 127,958,825-128,098,837 , GRCh37.p13 chr9: 130,721,104-130,861,116 EEIG1, NAIF1, 1 more genes
    nsv6869345copy number variation1nstd229human GRCh38 chr9: 127,951,402-128,083,324 , GRCh37.p13 chr9: 130,713,681-130,845,603 NAIF1, SLC25A25, 1 more genes
    nsv6860181copy number variation1nstd229human GRCh38 chr9: 128,058,001-128,071,700 , GRCh37.p13 chr9: 130,820,280-130,833,979 SLC25A25, NAIF1
    nsv6858409copy number variation1nstd229human GRCh38 chr9: 127,769,112-128,669,700 , GRCh37.p13 chr9: 130,531,391-131,431,979 BBLN, SH2D3C, 47 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
    nsv6633343copy number variation1nstd224human GRCh37 chr9: 130,778,514-130,851,573 , GRCh38.p12 chr9: 128,016,235-128,089,294 SLC25A25, NAIF1
    nsv6450991copy number variation1nstd223human GRCh38 chr9: 128,060,592-128,064,177 , GRCh37.p13 chr9: 130,822,871-130,826,456 NAIF1
    nsv6445830copy number variation1nstd223human GRCh38 chr9: 127,317,501-128,138,900 , GRCh37.p13 chr9: 130,079,780-130,901,179 STXBP1, PTGES2-AS1, 34 more genes
    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
    nsv6312681copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,216,807-130,953,136 , GRCh38.p12 chr9: 127,454,528-128,190,857 EEIG1, PIP5KL1, 32 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
    nsv6141806copy number variation1nstd206human GRCh38 chr9: 128,052,552-128,060,552 , GRCh37.p13 chr9: 130,814,831-130,822,831 NAIF1
    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
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5482551copy number variation1nstd206human GRCh38 chr9: 128,059,116-128,059,889 , GRCh37.p13 chr9: 130,821,395-130,822,168 NAIF1
    nsv5255143copy number variation1nstd204human GRCh38.p13 chr9: 128,000,401-128,091,700 , GRCh37.p13 chr9: 130,762,680-130,853,979 SLC25A25, NAIF1
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