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Items: 1 to 20 of 35

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3889024copy number variation1nstd102humanPathogenic GRCh38 chr14: 58,443,934-58,450,766 , GRCh37 chr14: 58,910,652-58,917,484 KIAA0586
    nsv7094438copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,938,897-58,941,535 , GRCh38.p12 chr14: 58,472,179-58,474,817 KIAA0586
    nsv7094437copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,926,541-58,927,898 , GRCh38.p12 chr14: 58,459,823-58,461,180 KIAA0586
    nsv7094502copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,975,253-58,975,447 , GRCh38.p12 chr14: 58,508,535-58,508,729 KIAA0586
    nsv7094501copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 58,951,496-58,953,792 , GRCh38.p12 chr14: 58,484,778-58,487,074 KIAA0586
    nsv7094500copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 58,910,652-58,917,484 , GRCh38.p12 chr14: 58,443,934-58,450,766 KIAA0586
    nsv7094338copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 58,896,061-58,899,195 , GRCh38.p12 chr14: 58,429,343-58,432,477 KIAA0586
    nsv4683893copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 58,915,038-58,917,484 , GRCh38.p12 chr14: 58,448,320-58,450,766 KIAA0586
    nsv7094339copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 58,949,211-58,949,450 , GRCh38.p12 chr14: 58,482,493-58,482,732 KIAA0586
    nsv7094436copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,910,652-58,910,913 , GRCh38.p12 chr14: 58,443,934-58,444,195 KIAA0586
    nsv7094340copy number variation1nstd102humanUncertain significance GRCh37 chr14: 59,010,581-59,014,694 , GRCh38.p12 chr14: 58,543,863-58,547,976 KIAA0586
    nsv7093242copy number variation1nstd102humanUncertain significance GRCh38 chr14: 58,429,375-58,429,376 , GRCh37 chr14: 58,896,093-58,896,094 KIAA0586
    nsv7094499copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,894,347-58,899,195 , GRCh38.p12 chr14: 58,427,629-58,432,477 KIAA0586, TIMM9
    nsv7094435copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,894,347-59,014,694 , GRCh38.p12 chr14: 58,427,629-58,547,976 KIAA0586, HSBP1P1, 2 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 KIAA0586, PARP1P2, 160 more genes
    nsv3924033copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999 KIAA0586, DACT1, 105 more genes
    nsv3915521copy number variation1nstd102humanPathogenic NCBI36 chr14: 57,682,493-60,810,090 , GRCh37 chr14: 58,612,740-61,740,337 , GRCh38 chr14: 58,146,022-61,273,619 KIAA0586, DACT1, 61 more genes
    nsv4674918copy number variation1nstd102humanPathogenic GRCh37 chr14: 56,605,398-59,404,256 , GRCh38.p12 chr14: 56,138,680-58,937,538 KIAA0586, RNU6-1204P, 42 more genes
    nsv6309551copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,711,639-59,014,694 , GRCh38.p12 chr14: 58,244,921-58,547,976 KIAA0586, LINC00216, 10 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 KIAA0586, LOC440181, 1998 more genes
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