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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141208copy number variation1nstd232human GRCh37.p13 chr4: 155,461,845-155,461,933 , GRCh38.p12 chr4: 154,540,693-154,540,781 PLRG1
    nsv7093377copy number variation1nstd102humannot provided GRCh37 chr4: 154,928,902-155,707,223 , GRCh38.p12 chr4|NW_017363814.1: 1-420,675 , GRCh38.p12 chr4: 154,007,750-154,786,071 FGA, FGG, 13 more genes
    nsv7048230inversion1nstd229human GRCh38 chr4: 149,781,104-157,324,460 , GRCh37.p13 chr4: 150,702,256-158,245,612 LOC107986197, LINC02273, 119 more genes
    nsv6752708copy number variation1nstd229human GRCh38 chr4: 154,489,292-154,803,489 , GRCh37.p13 chr4: 155,410,444-155,724,641 PLRG1, LOC105377500, 12 more genes
    nsv6750817copy number variation1nstd229human GRCh38 chr4: 154,013,779-154,793,137 , GRCh37.p13 chr4: 154,934,931-155,714,289 LRAT, RBM46, 14 more genes
    nsv6742949copy number variation1nstd229human GRCh38 chr4: 154,550,387-154,552,516 , GRCh37.p13 chr4: 155,471,539-155,473,668 PLRG1
    nsv6135259copy number variation1nstd213human GRCh37 chr4: 155,371,823-155,467,675 , GRCh38.p12 chr4: 154,450,671-154,546,523 PLRG1, DCHS2, 2 more genes
    nsv6134913copy number variation1nstd213human GRCh37 chr4: 155,140,000-155,510,001 , GRCh38.p12 chr4: 154,218,848-154,588,849 , GRCh38.p12 chr4|NW_017363814.1: 146,477-420,675 FGA, FGB, 7 more genes
    nsv6134911copy number variation1nstd213human GRCh37 chr4: 147,270,000-190,610,001 , GRCh38.p12 chr4: 146,348,848-189,688,847 , AGA, 517 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
    nsv6134723copy number variation1nstd213human GRCh37 chr4: 155,371,820-155,467,678 , GRCh38.p12 chr4: 154,450,668-154,546,526 PLRG1, DCHS2, 2 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
    nsv5574634copy number variation1nstd207human GRCh38 chr4: 154,475,275-154,538,487 , GRCh37.p13 chr4: 155,396,427-155,459,639 PLRG1, DCHS2, 1 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
    nsv5353310translocation1nstd200human GRCh38 chr4: 154,534,194-154,534,194 , GRCh38 chr4: 154,535,131-154,535,131 , GRCh37.p13 chr4: 155,455,346-155,455,346 , GRCh37.p13 chr4: 155,456,283-155,456,283 PLRG1
    nsv5089046mobile element insertion1nstd203human GRCh38 chr4: 154,541,745-154,541,760 , GRCh37.p13 chr4: 155,462,897-155,462,912 PLRG1
    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
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