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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899901copy number variation1nstd209human GRCh38 chr4: 118,692,501-118,752,790 , GRCh37.p13 chr4: 119,613,656-119,673,945 SEC24D, METTL14
    nsv5837324copy number variation1nstd209human GRCh38 chr4: 118,704,340-118,743,849 , GRCh37.p13 chr4: 119,625,495-119,665,004 SEC24D, METTL14
    nsv5837323copy number variation1nstd209human GRCh38 chr4: 118,692,530-118,700,879 , GRCh37.p13 chr4: 119,613,685-119,622,034 METTL14
    nsv5693075mobile element insertion1nstd211human GRCh38 chr4: 118,695,204-118,695,204 , GRCh37.p13 chr4: 119,616,359-119,616,359 METTL14
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5410140mobile element insertion1nstd206human GRCh38 chr4: 118,695,254-118,695,254 , GRCh37.p13 chr4: 119,616,409-119,616,409 METTL14
    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
    nsv5347047translocation1nstd200human GRCh38 chr4: 118,690,641-118,690,641 , GRCh38 chr4: 118,690,577-118,690,577 , GRCh37.p13 chr4: 119,611,732-119,611,732 , GRCh37.p13 chr4: 119,611,796-119,611,796 METTL14
    nsv4943909copy number variation1nstd200human GRCh38 chr4: 118,707,301-118,712,452 , GRCh37.p13 chr4: 119,628,456-119,633,607 METTL14
    nsv4935532copy number variation1nstd200human GRCh38 chr4: 118,712,985-118,717,104 , GRCh37.p13 chr4: 119,634,140-119,638,259 METTL14
    nsv4794439copy number variation1nstd200human GRCh37 chr4: 119,628,456-119,633,607 , GRCh38.p12 chr4: 118,707,301-118,712,452 METTL14
    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
    nsv4570863mobile element insertion1nstd166human GRCh37.p13 chr4: 119,623,157-119,623,157 , GRCh38.p12 chr4: 118,702,002-118,702,002 METTL14
    nsv4567711mobile element insertion1nstd166human GRCh37.p13 chr4: 119,624,774-119,624,774 , GRCh38.p12 chr4: 118,703,619-118,703,619 METTL14
    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
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