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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098424copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,578,196-130,581,131 , GRCh38.p12 chr9: 127,815,917-127,818,852 ENG, LOC102723566
    nsv7097927copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,578,196-130,582,336 , GRCh38.p12 chr9: 127,815,917-127,820,057 ENG, LOC102723566
    nsv7097688copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,579,418-130,579,492 , GRCh38.p12 chr9: 127,817,139-127,817,213 LOC102723566, ENG
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7065323inversion1nstd229human GRCh38 chr9: 127,814,774-127,814,903 , GRCh37.p13 chr9: 130,577,053-130,577,182 LOC102723566, ENG, 1 more genes
    nsv6875789copy number variation1nstd229human GRCh38 chr9: 127,789,399-127,824,185 , GRCh37.p13 chr9: 130,551,678-130,586,464 LOC102723566, CDK9, 3 more genes
    nsv6870410copy number variation1nstd229human GRCh38 chr9: 127,746,197-127,854,648 , GRCh37.p13 chr9: 130,508,476-130,616,927 ENG, RNA5SP296, 8 more genes
    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
    nsv6454446copy number variation1nstd223human GRCh38 chr9: 127,818,979-127,822,851 , GRCh37.p13 chr9: 130,581,258-130,585,130 ENG, LOC102723566
    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
    nsv6315517copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,581,787-130,582,459 , GRCh38.p12 chr9: 127,819,508-127,820,180 ENG, LOC102723566
    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
    nsv6312839copy number variation1nstd102humanUncertain significance GRCh37 chr9: 130,578,190-130,616,640 , GRCh38.p12 chr9: 127,815,911-127,854,361 LOC105379841, LOC102723566, 2 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
    nsv6289935copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,577,259-130,593,094 , GRCh38 chr9: 127,814,980-127,830,815 ENG, FPGS, 2 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
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