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Items: 1 to 20 of 523

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923501copy number variation1nstd209human GRCh38 chr11: 128,812,821-128,813,513 , GRCh37.p13 chr11: 128,682,716-128,683,408 FLI1
    nsv5662720insertion1nstd207human GRCh38 chr11: 128,695,049-128,695,049 , GRCh37.p13 chr11: 128,564,944-128,564,944 FLI1, SENCR
    nsv5603992copy number variation1nstd207human GRCh38 chr11: 128,812,821-128,813,513 , GRCh37.p13 chr11: 128,682,716-128,683,408 FLI1
    nsv5496641copy number variation1nstd206human GRCh38 chr11: 128,700,440-128,713,490 , GRCh37.p13 chr11: 128,570,335-128,583,385 FLI1
    nsv5495487copy number variation1nstd206human GRCh38 chr11: 128,812,821-128,813,515 , GRCh37.p13 chr11: 128,682,716-128,683,410 FLI1
    nsv5341011translocation1nstd200human GRCh37 chr11: 128,564,932-128,564,932 , GRCh37 chr11: 128,564,850-128,564,850 , GRCh38.p12 chr11: 128,695,037-128,695,037 , GRCh38.p12 chr11: 128,694,955-128,694,955 FLI1, SENCR
    nsv5304353copy number variation1nstd204human GRCh38.p13 chr11: 128,812,821-128,813,515 , GRCh37.p13 chr11: 128,682,716-128,683,410 FLI1
    nsv5261086copy number variation1nstd204human GRCh38.p13 chr11: 128,812,801-128,813,500 , GRCh37.p13 chr11: 128,682,696-128,683,395 FLI1
    nsv5127138mobile element insertion1nstd203human GRCh38 chr11: 128,711,639-128,711,650 , GRCh37.p13 chr11: 128,581,534-128,581,545 FLI1
    nsv5125009mobile element insertion1nstd203human GRCh38 chr11: 128,722,545-128,722,562 , GRCh37.p13 chr11: 128,592,440-128,592,457 FLI1
    nsv4981268copy number variation1nstd200human GRCh38 chr11: 128,812,821-128,813,515 , GRCh37.p13 chr11: 128,682,716-128,683,410 FLI1
    nsv4981267copy number variation1nstd200human GRCh38 chr11: 128,811,771-128,812,026 , GRCh37.p13 chr11: 128,681,666-128,681,921 FLI1
    nsv4981266copy number variation1nstd200human GRCh38 chr11: 128,712,086-128,713,301 , GRCh37.p13 chr11: 128,581,981-128,583,196 FLI1
    nsv4981265copy number variation1nstd200human GRCh38 chr11: 128,686,430-128,687,029 , GRCh37.p13 chr11: 128,556,325-128,556,924 FLI1, LOC101929538
    nsv4835062copy number variation1nstd200human GRCh37 chr11: 128,682,716-128,683,410 , GRCh38.p12 chr11: 128,812,821-128,813,515 FLI1
    nsv4737758copy number variation1nstd199human GRCh37 chr11: 128,682,714-128,683,406 , GRCh38.p12 chr11: 128,812,819-128,813,511 FLI1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4729245copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,683,017-128,897,053 , GRCh38.p12 chr11: 128,813,122-129,027,158 TP53AIP1, KCNJ5-AS1, 6 more genes
    nsv4729012copy number variation1nstd102humanPathogenic GRCh37 chr11: 127,602,115-134,938,470 , GRCh38.p12 chr11: 127,732,220-135,068,576 LINC02706, APLP2, 92 more genes
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 more genes
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