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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
    nsv7053923inversion1nstd229human GRCh38 chr4: 143,521,980-150,843,613 , GRCh37.p13 chr4: 144,443,133-151,764,765 AKIRIN2P1, PRMT9, 87 more genes
    nsv7050914inversion1nstd229human GRCh38 chr4: 143,519,295-150,840,265 , GRCh37.p13 chr4: 144,440,448-151,761,417 MIR548G, LOC100420464, 87 more genes
    nsv6756815copy number variation1nstd229human GRCh38 chr4: 146,389,167-146,885,089 , GRCh37.p13 chr4: 147,310,319-147,806,241 LOC105377474, POU4F2, 4 more genes
    nsv6746937copy number variation1nstd229human GRCh38 chr4: 146,640,401-146,644,600 , GRCh37.p13 chr4: 147,561,553-147,565,752 POU4F2
    nsv6740782copy number variation1nstd229human GRCh38 chr4: 146,639,901-146,642,600 , GRCh37.p13 chr4: 147,561,053-147,563,752 POU4F2
    nsv6740574copy number variation1nstd229human GRCh38 chr4: 146,582,400-146,744,983 , GRCh37.p13 chr4: 147,503,552-147,666,135 TTC29, POU4F2
    nsv6311715copy number variation1nstd102humanPathogenic GRCh37 chr4: 146,560,292-149,358,012 , GRCh38.p12 chr4: 145,639,140-148,436,860 PRMT5P1, LOC105377472, 32 more genes
    nsv6291328copy number variation1nstd102humanUncertain significance GRCh37 chr4: 147,319,707-147,970,747 , GRCh38.p12 chr4: 146,398,555-147,049,595 LOC105377474, LOC100996262, 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
    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
    nsv5901358copy number variation1nstd209human GRCh38 chr4: 146,639,312-146,639,374 , GRCh37.p13 chr4: 147,560,464-147,560,526 POU4F2
    nsv5896233copy number variation1nstd209human GRCh38 chr4: 146,190,128-146,855,608 , GRCh37.p13 chr4: 147,111,280-147,776,760 POU4F2, LSM6, 7 more genes
    nsv5838051copy number variation1nstd209human GRCh38 chr4: 146,640,539-146,672,116 , GRCh37.p13 chr4: 147,561,691-147,593,268 POU4F2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5353247translocation1nstd200human GRCh38 chr4: 146,639,375-146,639,375 , GRCh38 chr4: 146,639,322-146,639,322 , GRCh37.p13 chr4: 147,560,474-147,560,474 , GRCh37.p13 chr4: 147,560,527-147,560,527 POU4F2
    nsv4794557copy number variation1nstd200human GRCh37 chr4: 147,111,280-147,776,761 , GRCh38.p12 chr4: 146,190,128-146,855,609 LSM6, LOC105377472, 7 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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