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Items: 1 to 20 of 439

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3963721copy number variation1nstd168human GRCh38 (hg38) chr15: 39,948,007-39,987,997 , GRCh37.p13 chr15: 40,240,208-40,280,198 EIF2AK4, H3F3AP1
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr12: 115,131,583-133,166,920 , GRCh37.p13 chr12: 115,569,388-133,743,506 , NCBI36 (hg18) chr12: 114,053,771-132,253,579 BCL7A, SCARB1, 386 more genes
    nsv3923477copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr15: 39,710,935-40,294,591 , GRCh37.p13 chr15: 40,003,136-40,586,792 , NCBI36 (hg18) chr15: 37,790,428-38,374,084 EIF2AK4, PLCB2, 17 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 EIF2AK4, ACTBP7, 1440 more genes
    nsv3922077copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr12: 119,286,893-122,638,552 , GRCh37.p13 chr12: 119,724,698-123,123,099 , NCBI36 (hg18) chr12: 118,209,081-121,689,052 MSI1, PRKAB1, 96 more genes
    nsv3920626copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr15: 36,531,993-40,787,538 , GRCh37.p13 chr15: 36,824,194-41,079,736 , NCBI36 (hg18) chr15: 34,611,486-38,867,028 EIF2AK4, RASGRP1, 79 more genes
    nsv3920557copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr12: 118,165,459-133,182,322 , GRCh37.p13 chr12: 118,603,264-133,758,908 , NCBI36 (hg18) chr12: 117,087,647-132,268,981 POLE, PRKAB1, 348 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 EIF2AK4, ANPEP, 1505 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 EIF2AK4, ANXA2, 1715 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 EIF2AK4, ADAM10, 1712 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 EIF2AK4, ACTBP7, 1684 more genes
    nsv3915967copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr15: 32,635,803-40,233,825 , GRCh37.p13 chr15: 32,928,004-40,526,026 , NCBI36 (hg18) chr15: 30,715,296-38,313,318 EIF2AK4, ACTC1, 117 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 EIF2AK4, ALDH1A3, 1491 more genes
    nsv3914194copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr12: 121,271-133,196,807 , GRCh37.p13 chr12: 282,465-133,773,393 , NCBI36 (hg18) chr12: 100,698-132,283,466 ACVRL1, ABCD2, 2517 more genes
    nsv3913894copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr12: 114,268,403-133,201,316 , GRCh37.p13 chr12: 114,706,208-133,777,902 , NCBI36 (hg18) chr12: 113,190,591-132,287,975 COX6A1, EIF2B1, 397 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 EIF2AK4, ACTBP7, 1826 more genes
    nsv3911945copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 EIF2AK4, ACTBP7, 1718 more genes
    nsv3906446copy number variation1nstd102humanLikely pathogenic GRCh37 (hg19) chr12: 118,486,842-120,995,382 , GRCh38.p12 chr12: 118,049,037-120,557,579 , NCBI36 (hg18) chr12: 116,971,225-119,479,765 PLA2G1B, SRSF9, 64 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , NCBI36 (hg18) chr12: 44,048-132,287,975 A2MP1, ACACB, 2518 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 , NCBI36 (hg18) chr15: 18,993,409-100,329,139 EIF2AK4, ALDH1A3, 1809 more genes
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