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Items: 1 to 20 of 177

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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
    nsv5689962mobile element insertion1nstd211human GRCh38 chr4: 140,424,550-140,424,550 , GRCh37.p13 chr4: 141,345,704-141,345,704 CLGN
    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
    nsv5407869mobile element insertion1nstd206human GRCh38 chr4: 140,424,550-140,424,601 , GRCh37.p13 chr4: 141,345,704-141,345,755 CLGN
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5239390copy number variation1nstd204human GRCh38.p13 chr4: 140,416,501-140,417,100 , GRCh37.p13 chr4: 141,337,655-141,338,254 CLGN
    nsv5233277copy number variation1nstd204human GRCh38.p13 chr4: 140,403,765-140,405,214 , GRCh37.p13 chr4: 141,324,919-141,326,368 CLGN
    nsv5233089copy number variation1nstd204human GRCh38.p13 chr4: 140,409,401-140,412,600 , GRCh37.p13 chr4: 141,330,555-141,333,754 CLGN
    nsv5096950mobile element insertion1nstd203human GRCh38 chr4: 140,422,517-140,422,532 , GRCh37.p13 chr4: 141,343,671-141,343,686 CLGN
    nsv5090761mobile element insertion1nstd203human GRCh38 chr4: 140,405,191-140,405,202 , GRCh37.p13 chr4: 141,326,345-141,326,356 CLGN
    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
    nsv4456879copy number variation1nstd102humanUncertain significance GRCh37 chr4: 134,054,911-142,601,496 , GRCh38.p12 chr4: 133,133,756-141,680,343 NOCT, IL15, 81 more genes
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