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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978819inversion1nstd209human GRCh38 chr15: 81,455,809-83,007,946 , GRCh37.p13 chr15: 81,748,150-83,676,698 RPS17, AP3B2, 39 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5272780copy number variation1nstd204human GRCh38.p13 chr15: 82,538,017-82,540,050 , GRCh37.p13 chr15: 82,822,425-82,824,458 RPS17
    nsv5002034copy number variation1nstd200human GRCh38 chr15: 82,528,523-82,536,607 , GRCh37.p13 chr15: 82,812,931-82,821,015 DNM1P38, RPS17
    nsv4628057copy number variation1nstd183human GRCh37 chr15: 83,100,333-83,214,286 , GRCh38.p12 chr15|NT_187606.1: 220,688-334,641 , GRCh38.p12 chr15: 82,431,603-82,545,536 GOLGA2P10, DNM1P36, 10 more genes
    nsv4625888copy number variation1nstd183human GRCh37 chr15: 83,108,458-83,315,731 , GRCh38.p12 chr15: 82,439,733-82,641,774 , GRCh38.p12 chr15|NT_187606.1: 228,813-430,880 , RPS17, 11 more genes
    nsv4620937copy number variation1nstd183human GRCh37 chr15: 82,724,066-82,825,198 , GRCh38.p12 chr15: 82,431,865-82,540,790 DNM1P36, GOLGA2P10, 8 more genes
    nsv4456897copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,468,371-84,797,068 , GRCh38.p12 chr15: 82,176,030-84,128,316 HDGFL3, LOC105370926, 46 more genes
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 LOC100288241, LOC105370926, 64 more genes
    nsv4455892copy number variation1nstd102humanPathogenic GRCh37 chr15: 82,688,216-84,796,779 , GRCh38.p12 chr15: 82,396,005-84,128,027 UBE2Q2P2, GOLGA2P10, 40 more genes
    nsv4421723copy number variation1nstd174human GRCh37 chr15: 83,108,446-83,315,731 , GRCh38.p12 chr15: 82,439,721-82,641,774 , GRCh38.p12 chr15|NT_187606.1: 228,801-430,880 , CSPG4P10, 11 more genes
    nsv4418339copy number variation1nstd174human GRCh37 chr15: 82,693,587-82,829,609 , GRCh38.p12 chr15: 82,401,376-82,545,201 CPEB1, GOLGA2P10, 10 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 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 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 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 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 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 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 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 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 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 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 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 RPL21P113, LOC112268152, 1428 more genes
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