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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4922728copy number variation1nstd200human GRCh38 chr4: 66,431,100-66,431,162 , GRCh37.p13 chr4: 67,296,818-67,296,880 RPS23P3
    nsv4922723copy number variation1nstd200human GRCh38 chr4: 66,275,389-66,565,011 , GRCh37.p13 chr4: 67,141,107-67,430,729 MIR1269A, RPS23P3
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    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
    nsv4674399copy number variation1nstd102humanUncertain significance GRCh37 chr4: 66,948,561-69,631,390 , GRCh38.p12 chr4: 66,082,843-68,765,672 RNA5SP527, LOC100419046, 42 more genes
    nsv4589055copy number variation1nstd183human GRCh37 chr4: 66,868,306-67,323,374 , GRCh38.p12 chr4: 66,002,588-66,457,656 RPS23P3, MIR1269A, 2 more genes
    nsv4436051copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 61,605,456-68,762,943 , GRCh38.p12 chr4: 60,739,738-67,897,225 CENPC, EPHA5, 60 more genes
    nsv4317585inversion1nstd166human GRCh37.p13 chr4: 57,479,624-69,003,923 , GRCh38.p12 chr4: 56,613,458-68,138,205 CENPC, GNRHR, 98 more genes
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 EREG, EFL1P2, 530 more genes
    nsv3919919copy number variation1nstd102humanUncertain significance NCBI36 chr4: 66,006,724-68,731,977 , GRCh37.p13 chr4: 66,324,129-69,049,382 , GRCh38.p12 chr4: 65,458,411-68,183,664 CENPC, LOC100419862, 37 more genes
    nsv3918216copy number variation1nstd102humanUncertain significance GRCh38 chr4: 65,873,016-68,743,024 , GRCh37 chr4: 66,738,734-69,608,742 , NCBI36 chr4: 66,421,329-69,643,331 UBA6-DT, MT2P1, 45 more genes
    nsv3915772copy number variation1nstd102humanUncertain significance NCBI36 chr4: 66,812,047-67,087,677 , GRCh37.p13 chr4: 67,129,452-67,405,082 , GRCh38.p12 chr4: 66,263,734-66,539,364 MIR1269A, RPS23P3
    nsv3914714copy number variation1nstd102humanUncertain significance GRCh37 chr4: 67,006,250-67,842,152 , GRCh38 chr4: 66,140,532-66,976,434 , NCBI36 chr4: 66,688,845-67,524,747 RPS23P3, LOC105377262, 2 more genes
    nsv3913811copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792 LOC105377297, HNRNPA1P56, 582 more genes
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