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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906320copy number variation1nstd209human GRCh38 chr4: 56,912,715-56,912,998 , GRCh37.p13 chr4: 57,778,881-57,779,164 REST
    nsv5904014copy number variation1nstd209human GRCh38 chr4: 56,917,940-56,918,244 , GRCh37.p13 chr4: 57,784,106-57,784,410 REST
    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
    nsv5579591copy number variation1nstd207human GRCh38 chr4: 56,917,940-56,918,244 , GRCh37.p13 chr4: 57,784,106-57,784,410 REST
    nsv5461963copy number variation1nstd206human GRCh38 chr4: 56,917,940-56,918,237 , GRCh37.p13 chr4: 57,784,106-57,784,403 REST
    nsv5352974translocation1nstd200human GRCh38 chr4: 56,917,940-56,917,940 , GRCh38 chr4: 56,918,237-56,918,237 , GRCh37.p13 chr4: 57,784,403-57,784,403 , GRCh37.p13 chr4: 57,784,106-57,784,106 REST
    nsv5333468translocation1nstd200human GRCh37 chr4: 57,784,403-57,784,403 , GRCh37 chr4: 57,784,106-57,784,106 , GRCh38.p12 chr4: 56,917,940-56,917,940 , GRCh38.p12 chr4: 56,918,237-56,918,237 REST
    nsv5099626mobile element insertion1nstd203human GRCh38 chr4: 56,928,620-56,928,646 , GRCh37.p13 chr4: 57,794,786-57,794,812 REST
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4913423copy number variation1nstd200human GRCh38 chr4: 56,935,968-56,944,630 , GRCh37.p13 chr4: 57,802,134-57,810,796 REST
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4791910copy number variation1nstd200human GRCh37 chr4: 57,802,134-57,810,796 , GRCh38.p12 chr4: 56,935,968-56,944,630 REST
    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
    nsv4729168copy number variation1nstd102humanUncertain significance GRCh37 chr4: 57,588,857-57,872,994 , GRCh38.p12 chr4: 56,722,691-57,006,828 SPINK2, RN7SL492P, 7 more genes
    nsv4673993copy number variation1nstd102humanUncertain significance GRCh37 chr4: 57,067,953-57,957,651 , GRCh38.p12 chr4: 56,201,787-57,091,485 LOC285453, PPAT, 27 more genes
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