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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971187insertion1nstd209human GRCh38 chr15: 56,002,975-56,002,975 , GRCh37.p13 chr15: 56,295,173-56,295,173 CNOT6LP1
    nsv5928470copy number variation1nstd209human GRCh38 chr15: 56,007,198-56,028,317 , GRCh37.p13 chr15: 56,299,396-56,320,515 CNOT6LP1, RN7SL568P
    nsv5851515copy number variation1nstd209human GRCh38 chr15: 56,007,604-56,027,566 , GRCh37.p13 chr15: 56,299,802-56,319,764 CNOT6LP1
    nsv5650990insertion1nstd207human GRCh38 chr15: 56,007,282-56,007,282 , GRCh37.p13 chr15: 56,299,480-56,299,480 CNOT6LP1
    nsv5599263copy number variation1nstd207human GRCh38 chr15: 56,007,282-56,007,353 , GRCh37.p13 chr15: 56,299,480-56,299,551 CNOT6LP1
    nsv5522496copy number variation1nstd206human GRCh38 chr15: 55,988,962-56,009,986 , GRCh37.p13 chr15: 56,281,160-56,302,184 NEDD4, CNOT6LP1
    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
    nsv5158984mobile element insertion1nstd203human GRCh38 chr15: 56,002,007-56,002,025 , GRCh37.p13 chr15: 56,294,205-56,294,223 CNOT6LP1
    nsv5156342mobile element insertion1nstd203human GRCh38 chr15: 56,002,501-56,002,512 , GRCh37.p13 chr15: 56,294,699-56,294,710 CNOT6LP1
    nsv5149022mobile element insertion1nstd203human GRCh38 chr15: 56,002,977-56,002,995 , GRCh37.p13 chr15: 56,295,175-56,295,193 CNOT6LP1
    nsv5147466mobile element insertion1nstd203human GRCh38 chr15: 56,002,995-56,003,003 , GRCh37.p13 chr15: 56,295,193-56,295,201 CNOT6LP1
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4674858copy number variation1nstd102humanUncertain significance GRCh37 chr15: 56,186,664-56,370,552 , GRCh38.p12 chr15: 55,894,466-56,078,354 RN7SL568P, CD24P2, 2 more genes
    nsv4621527copy number variation2nstd183human GRCh37 chr15: 56,277,435-56,349,576 , GRCh38.p12 chr15: 55,985,237-56,057,378 NEDD4, CNOT6LP1, 1 more genes
    nsv4499043mobile element insertion1nstd166human GRCh37.p13 chr15: 56,295,170-56,295,170 , GRCh38.p12 chr15: 56,002,972-56,002,972 CNOT6LP1
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4455359copy number variation1nstd102humanPathogenic GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199 MIR4716, RPS13P8, 112 more genes
    nsv4413254copy number variation1nstd174human GRCh37 chr15: 56,210,318-56,426,501 , GRCh38.p12 chr15: 55,918,120-56,134,303 CD24P2, NEDD4, 3 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
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