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Items: 1 to 20 of 80

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv6953870copy number variation1nstd229human GRCh38 chr14: 23,639,903-23,659,521 , GRCh37.p13 chr14: 24,109,112-24,128,730 LOC105370407, DHRS2
    nsv6947579copy number variation1nstd229human GRCh38 chr14: 23,632,756-23,633,880 , GRCh37.p13 chr14: 24,101,965-24,103,089 DHRS2
    nsv6941203copy number variation1nstd229human GRCh38 chr14: 23,624,823-23,632,727 , GRCh37.p13 chr14: 24,094,032-24,101,936 DHRS2
    nsv6491302copy number variation1nstd223human GRCh38 chr14: 23,639,903-23,659,521 , GRCh37.p13 chr14: 24,109,112-24,128,730 DHRS2, LOC105370407
    nsv6484983copy number variation1nstd223human GRCh38 chr14: 23,632,493-23,633,880 , GRCh37.p13 chr14: 24,101,702-24,103,089 DHRS2
    nsv6483044copy number variation1nstd223human GRCh38 chr14: 23,629,282-23,631,102 , GRCh37.p13 chr14: 24,098,491-24,100,311 DHRS2
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6291592copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,080,271-24,152,531 , GRCh38.p12 chr14: 23,611,062-23,683,322 LOC105370407, DHRS2
    nsv6132775copy number variation1nstd213human GRCh37 chr14: 22,590,000-24,410,001 , GRCh38.p12 chr14: 22,122,042-23,940,792 BCL2L2, CEBPE, 167 more genes
    nsv5561752sequence alteration1nstd206human GRCh38 chr14: 23,629,192-23,629,195 , GRCh37.p13 chr14: 24,098,401-24,098,404 DHRS2
    nsv5497432copy number variation1nstd206human GRCh38 chr14: 23,632,719-23,633,919 , GRCh37.p13 chr14: 24,101,928-24,103,128 DHRS2
    nsv5318939copy number variation1nstd204human GRCh38.p13 chr14: 23,632,747-23,633,884 , GRCh37.p13 chr14: 24,101,956-24,103,093 DHRS2
    nsv5185220mobile element insertion1nstd203human GRCh38 chr14: 23,635,507-23,635,523 , GRCh37.p13 chr14: 24,104,716-24,104,732 DHRS2
    nsv4990868copy number variation1nstd200human GRCh38 chr14: 23,632,755-23,633,879 , GRCh37.p13 chr14: 24,101,964-24,103,088 DHRS2
    nsv4842147copy number variation1nstd200human GRCh37 chr14: 24,101,964-24,103,088 , GRCh38.p12 chr14: 23,632,755-23,633,879 DHRS2
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
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