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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5516159copy number variation1nstd206human GRCh38 chr15: 82,880,664-83,048,892 , GRCh37.p13 chr15: 83,549,416-83,717,644 HOMER2, BTBD1, 4 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
    nsv4729284copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,201,955-85,786,847 , GRCh38.p12 chr15: 82,641,775-85,243,616 GOLGA6L5P, DNM1P44, 77 more genes
    nsv4578262copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,214,012-84,772,030 , GRCh38.p12 chr15: 82,641,775-84,103,278 LOC100421235, LOC105370933, 29 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
    nsv4246908copy number variation1nstd166human GRCh37.p13 chr15: 83,711,001-83,715,272 , GRCh38.p12 chr15: 83,042,249-83,046,520 FABP5P8, BTBD1
    nsv3964244copy number variation1nstd168human GRCh38 chr15: 83,018,513-83,064,183 , GRCh37.p13 chr15: 83,687,265-83,732,935 BTBD1, FABP5P8
    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
    nsv3921160copy number variation1nstd102humanPathogenic NCBI36 chr15: 81,011,067-82,580,838 , GRCh38 chr15: 82,558,402-84,121,082 , GRCh37 chr15: 83,214,012-84,789,834 HDGFL3, ACTG1P17, 29 more genes
    nsv3920008copy number variation1nstd102humanLikely pathogenic NCBI36 chr15: 81,026,720-83,529,848 , GRCh37 chr15: 83,229,665-85,728,844 , GRCh38 chr15: 82,560,915-85,185,613 BNC1, NMB, 71 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
    nsv3916778copy number variation1nstd102humanLikely pathogenic NCBI36 chr15: 80,880,473-83,587,851 , GRCh37 chr15: 83,083,418-85,786,847 , GRCh38 chr15: 82,627,214-85,243,616 BNC1, NMB, 77 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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