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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5570299copy number variation1nstd207human GRCh38 chr4: 118,671,407-118,671,747 , GRCh37.p13 chr4: 119,592,562-119,592,902 METTL14-DT
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5545494insertion1nstd206human GRCh38 chr4: 118,681,414-118,681,452 , GRCh37.p13 chr4: 119,602,569-119,602,607 METTL14-DT
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5367784translocation1nstd200human GRCh38 chr4: 118,679,105-118,679,105 , GRCh38 chr4: 118,673,463-118,673,463 , GRCh37.p13 chr4: 119,594,618-119,594,618 , GRCh37.p13 chr4: 119,600,260-119,600,260 METTL14-DT
    nsv5367783translocation1nstd200human GRCh38 chr4: 118,673,456-118,673,456 , GRCh38 chr4: 118,673,987-118,673,987 , GRCh37.p13 chr4: 119,595,142-119,595,142 , GRCh37.p13 chr4: 119,594,611-119,594,611 METTL14-DT
    nsv4943908copy number variation1nstd200human GRCh38 chr4: 118,584,045-118,669,725 , GRCh37.p13 chr4: 119,505,200-119,590,880 RNU6-1054P, CICP16, 3 more genes
    nsv4808183copy number variation1nstd200human GRCh37 chr4: 119,594,208-119,595,232 , GRCh38.p12 chr4: 118,673,053-118,674,077 METTL14-DT
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4589677copy number variation1nstd183human GRCh37 chr4: 119,585,241-119,586,148 , GRCh38.p12 chr4: 118,664,086-118,664,993 METTL14-DT
    nsv4589676copy number variation1nstd183human GRCh37 chr4: 119,552,399-119,584,340 , GRCh38.p12 chr4: 118,631,244-118,663,185 LOC729218, METTL14-DT, 2 more genes
    nsv4589674copy number variation2nstd183human GRCh37 chr4: 119,519,085-119,598,031 , GRCh38.p12 chr4: 118,597,930-118,676,876 RNU6-1054P, LOC729218, 3 more genes
    nsv4549319insertion1nstd166human GRCh37.p13 chr4: 119,602,562-119,602,562 , GRCh38.p12 chr4: 118,681,407-118,681,407 METTL14-DT
    nsv4521513copy number variation1nstd166human GRCh37.p13 chr4: 119,424,999-119,929,000 , GRCh38.p12 chr4: 118,503,844-119,007,845 CEP170P1, SEC24D, 9 more genes
    nsv4456441copy number variation1nstd102humanUncertain significance GRCh37 chr4: 119,410,381-119,730,068 , GRCh38.p12 chr4: 118,489,226-118,808,913 LOC105379403, CEP170P1, 7 more genes
    nsv4436254copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 116,624,547-126,168,646 , GRCh38.p12 chr4: 115,703,391-125,247,491 ANXA5, CCNA2, 125 more genes
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