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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6750001copy number variation1nstd229human GRCh38 chr4: 143,426,095-143,431,968 , GRCh37.p13 chr4: 144,347,248-144,353,121 RPSAP36, GAB1
    nsv6745295copy number variation1nstd229human GRCh38 chr4: 143,422,701-143,435,300 , GRCh37.p13 chr4: 144,343,854-144,356,453 GAB1, RPSAP36
    nsv6745129copy number variation1nstd229human GRCh38 chr4: 143,335,197-143,467,175 , GRCh37.p13 chr4: 144,256,350-144,388,328 MIR3139, GAB1, 2 more genes
    nsv6738881copy number variation1nstd229human GRCh38 chr4: 142,775,537-143,579,279 , GRCh37.p13 chr4: 143,696,690-144,500,432 USP38, USP38-DT, 11 more genes
    nsv6738263copy number variation1nstd229human GRCh38 chr4: 143,425,227-143,432,667 , GRCh37.p13 chr4: 144,346,380-144,353,820 RPSAP36, GAB1
    nsv6629362copy number variation1nstd224human GRCh37 chr4: 144,339,878-144,405,647 , GRCh38.p12 chr4: 143,418,725-143,484,494 GAB1, RPSAP36
    nsv6378471copy number variation1nstd223human GRCh38 chr4: 140,215,978-145,835,229 , GRCh37.p13 chr4: 141,137,132-146,756,381 OTUD4, GYPA, 62 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313656copy number variation1nstd102humanUncertain significance GRCh37 chr4: 136,035,308-144,718,930 , GRCh38.p12 chr4: 135,114,153-143,797,777 RPS2P20, LOC105377444, 87 more genes
    nsv6291168copy number variation1nstd102humanPathogenic GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146 LOC105377447, RN7SKP253, 92 more genes
    nsv6135295copy number variation1nstd213human GRCh37 chr4: 142,570,000-144,930,001 , GRCh38.p12 chr4: 141,648,847-144,008,848 GAB1, GYPE, 22 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 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
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