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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940619copy number variation1nstd209human GRCh38 chr14: 41,756,659-48,371,099 , GRCh37.p13 chr14: 42,225,862-48,840,302 LOC100418768, RNU6-297P, 53 more genes
    nsv5506794copy number variation1nstd206human GRCh38 chr14: 45,640,507-45,722,108 , GRCh37.p13 chr14: 46,109,710-46,191,311 LINC02303, LOC107984644
    nsv5301485copy number variation1nstd204human GRCh38.p13 chr14: 45,713,823-45,716,089 , GRCh37.p13 chr14: 46,183,026-46,185,292 LINC02303
    nsv5262270copy number variation1nstd204human GRCh38.p13 chr14: 45,713,114-45,716,110 , GRCh37.p13 chr14: 46,182,317-46,185,313 LINC02303
    nsv4999140copy number variation1nstd200human GRCh38 chr14: 45,713,803-45,716,106 , GRCh37.p13 chr14: 46,183,006-46,185,309 LINC02303
    nsv4999139copy number variation1nstd200human GRCh38 chr14: 45,712,647-45,712,885 , GRCh37.p13 chr14: 46,181,850-46,182,088 LINC02303
    nsv4999138copy number variation1nstd200human GRCh38 chr14: 45,690,890-45,726,812 , GRCh37.p13 chr14: 46,160,093-46,196,015 LOC107984644, LINC02303
    nsv4848884copy number variation1nstd200human GRCh37 chr14: 46,183,033-46,185,286 , GRCh38.p12 chr14: 45,713,830-45,716,083 LINC02303
    nsv4844259copy number variation1nstd200human GRCh37 chr14: 43,998,688-46,847,593 , GRCh38.p12 chr14: 43,529,485-46,378,390 RNU6-552P, C14orf28, 32 more genes
    nsv4843134copy number variation1nstd200human GRCh37 chr14: 46,160,093-46,196,015 , GRCh38.p12 chr14: 45,690,890-45,726,812 LINC02303, LOC107984644
    nsv4836801copy number variation1nstd200human GRCh37 chr14: 46,121,952-46,228,368 , GRCh38.p12 chr14: 45,652,749-45,759,165 LOC105370478, LOC107984644, 1 more genes
    nsv4769368copy number variation1nstd102humanUncertain significance GRCh37 chr14: 45,528,916-46,473,581 , GRCh38.p12 chr14: 45,059,713-46,004,378 RNU6-552P, MIS18BP1, 14 more genes
    nsv4675467copy number variation1nstd102humanLikely benign GRCh37 chr14: 45,361,304-46,896,735 , GRCh38.p12 chr14: 44,892,101-46,427,532 FANCM, TOGARAM1, 18 more genes
    nsv4414106copy number variation1nstd174human GRCh37 chr14: 46,108,235-46,231,045 , GRCh38.p12 chr14: 45,639,032-45,761,842 LINC02303, LOC107984644, 1 more genes
    nsv4369611copy number variation1nstd173human GRCh37 chr14: 45,764,082-46,505,829 , GRCh38.p12 chr14: 45,294,879-46,036,626 LOC105370475, LOC105370476, 4 more genes
    nsv4320386insertion1nstd166human GRCh37.p13 chr14: 46,176,092-46,176,092 , GRCh38.p12 chr14: 45,706,889-45,706,889 LINC02303
    nsv4231527copy number variation1nstd166human GRCh37.p13 chr14: 46,180,490-46,183,456 , GRCh38.p12 chr14: 45,711,287-45,714,253 LINC02303
    nsv4224510copy number variation1nstd166human GRCh37.p13 chr14: 45,706,735-46,434,494 , GRCh38.p12 chr14: 45,237,532-45,965,291 DNAJC19P9, LOC105378177, 8 more genes
    nsv4217033copy number variation1nstd166human GRCh37.p13 chr14: 46,118,025-46,735,975 , GRCh38.p12 chr14: 45,648,822-46,266,772 LINC02303, LOC105378177, 3 more genes
    nsv4216858copy number variation1nstd166human GRCh37.p13 chr14: 46,181,779-46,237,149 , GRCh38.p12 chr14: 45,712,576-45,767,946 LOC105370478, LINC02303
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