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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5954100insertion1nstd209human GRCh38 chr4: 140,565,830-140,565,830 , GRCh37.p13 chr4: 141,486,984-141,486,984 UCP1
    nsv5686553mobile element insertion1nstd211human GRCh38 chr4: 140,566,826-140,566,826 , GRCh37.p13 chr4: 141,487,980-141,487,980 UCP1
    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
    nsv5535058insertion1nstd206human GRCh38 chr4: 140,565,829-140,565,831 , GRCh37.p13 chr4: 141,486,983-141,486,985 UCP1
    nsv5409188mobile element insertion1nstd206human GRCh38 chr4: 140,566,826-140,566,877 , GRCh37.p13 chr4: 141,487,980-141,488,031 UCP1
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5237516copy number variation1nstd204human GRCh38.p13 chr4: 140,550,501-140,554,300 , GRCh37.p13 chr4: 141,471,655-141,475,454 UCP1, ELMOD2
    nsv4946028copy number variation1nstd200human GRCh38 chr4: 140,559,221-140,602,324 , GRCh37.p13 chr4: 141,480,375-141,523,478 UCP1, RN7SL152P
    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
    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
    nsv4674743copy number variation1nstd102humanPathogenic GRCh37 chr4: 137,901,978-141,527,647 , GRCh38.p12 chr4: 136,980,824-140,606,493 RAB33B-AS1, PPP1R14BP3, 56 more genes
    nsv4674499copy number variation1nstd102humanPathogenic GRCh37 chr4: 139,531,815-146,095,109 , GRCh38.p12 chr4: 138,610,661-145,173,957 GUSBP5, LOC100287014, 77 more genes
    nsv4555998insertion1nstd166human GRCh37.p13 chr4: 141,486,983-141,486,983 , GRCh38.p12 chr4: 140,565,829-140,565,829 UCP1
    nsv4473649mobile element insertion1nstd166human GRCh37.p13 chr4: 141,477,655-141,477,655 , GRCh38.p12 chr4: 140,556,501-140,556,501 UCP1
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