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Items: 1 to 20 of 352

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076935inversion1nstd229human GRCh38 chr9: 92,944,628-92,956,028 , GRCh37.p13 chr9: 95,706,910-95,718,310 FGD3
    nsv7063034inversion1nstd229human GRCh38 chr9: 92,942,258-92,954,528 , GRCh37.p13 chr9: 95,704,540-95,716,810 FGD3
    nsv6876821copy number variation1nstd229human GRCh38 chr9: 92,958,383-92,972,395 , GRCh37.p13 chr9: 95,720,665-95,734,677 FGD3
    nsv6876323copy number variation1nstd229human GRCh38 chr9: 92,980,719-92,981,116 , GRCh37.p13 chr9: 95,743,001-95,743,398 FGD3
    nsv6873651copy number variation1nstd229human GRCh38 chr9: 92,993,415-93,001,342 , GRCh37.p13 chr9: 95,755,697-95,763,624 FGD3
    nsv6872958copy number variation1nstd229human GRCh38 chr9: 92,966,661-92,970,336 , GRCh37.p13 chr9: 95,728,943-95,732,618 FGD3
    nsv6869009copy number variation1nstd229human GRCh38 chr9: 92,989,177-92,991,498 , GRCh37.p13 chr9: 95,751,459-95,753,780 FGD3
    nsv6868305copy number variation1nstd229human GRCh38 chr9: 92,872,501-93,049,600 , GRCh37.p13 chr9: 95,634,783-95,811,882 LOC642943, FGD3, 4 more genes
    nsv6867422copy number variation1nstd229human GRCh38 chr9: 92,963,414-92,967,103 , GRCh37.p13 chr9: 95,725,696-95,729,385 FGD3
    nsv6864780copy number variation1nstd229human GRCh38 chr9: 93,035,801-93,046,400 , GRCh37.p13 chr9: 95,798,083-95,808,682 FGD3
    nsv6862884copy number variation1nstd229human GRCh38 chr9: 92,943,337-92,971,796 , GRCh37.p13 chr9: 95,705,619-95,734,078 FGD3
    nsv6862107copy number variation1nstd229human GRCh38 chr9: 92,976,901-93,001,300 , GRCh37.p13 chr9: 95,739,183-95,763,582 FGD3
    nsv6860237copy number variation1nstd229human GRCh38 chr9: 92,943,040-92,947,197 , GRCh37.p13 chr9: 95,705,322-95,709,479 FGD3
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 more genes
    nsv6637275copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,649,997-95,850,428 , GRCh38.p12 chr9: 92,887,715-93,088,146 ALOX15P2, LOC101927954, 4 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
    nsv6569750inversion1nstd223human GRCh38 chr9: 92,980,322-92,980,688 , GRCh37.p13 chr9: 95,742,604-95,742,970 FGD3
    nsv6558975inversion1nstd223human GRCh38 chr9: 92,942,258-92,954,528 , GRCh37.p13 chr9: 95,704,540-95,716,810 FGD3
    nsv6452913copy number variation1nstd223human GRCh38 chr9: 93,009,401-93,011,500 , GRCh37.p13 chr9: 95,771,683-95,773,782 LOC101927954, FGD3
    nsv6449719copy number variation1nstd223human GRCh38 chr9: 93,009,224-93,012,115 , GRCh37.p13 chr9: 95,771,506-95,774,397 FGD3, LOC101927954
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