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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6753218copy number variation1nstd229human GRCh38 chr4: 133,868,202-138,044,340 , GRCh37.p13 chr4: 134,789,357-138,965,494 SERF1AP1, LOC105377442, 28 more genes
    nsv6743763copy number variation1nstd229human GRCh38 chr4: 137,404,209-137,866,219 , GRCh37.p13 chr4: 138,325,363-138,787,373 LOC101927414, LINC02172, 7 more genes
    nsv6739095copy number variation1nstd229human GRCh38 chr4: 137,517,998-137,518,689 , GRCh37.p13 chr4: 138,439,152-138,439,843 PCDH18
    nsv6377406copy number variation1nstd223human GRCh38 chr4: 137,523,021-137,523,556 , GRCh37.p13 chr4: 138,444,175-138,444,710 PCDH18
    nsv6375713copy number variation1nstd223human GRCh38 chr4: 137,525,336-137,525,976 , GRCh37.p13 chr4: 138,446,490-138,447,130 PCDH18
    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
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 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
    nsv6290718copy number variation1nstd102humanPathogenic GRCh37 chr4: 136,529,470-141,564,812 , GRCh38.p12 chr4: 135,608,315-140,643,658 MGARP, NAA15, 61 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
    nsv5979034inversion1nstd209human GRCh38 chr4: 136,299,558-138,570,240 , GRCh37.p13 chr4: 137,220,713-139,491,394 SLC7A11, PCDH18, 20 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
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv4873391inversion1nstd200human GRCh37 chr4: 137,941,721-143,237,901 , GRCh38.p12 chr4: 137,020,567-142,316,748 , MAML3, 68 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
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