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Items: 1 to 20 of 205

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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
    nsv7047764inversion1nstd229human GRCh38 chr4: 144,681,819-145,112,611 , GRCh37.p13 chr4: 145,602,971-146,033,763 ANAPC10, HHIP, 3 more genes
    nsv6749817copy number variation1nstd229human GRCh38 chr4: 145,128,617-145,128,785 , GRCh37.p13 chr4: 146,049,769-146,049,937 ABCE1
    nsv6749194copy number variation1nstd229human GRCh38 chr4: 144,985,079-145,110,608 , GRCh37.p13 chr4: 145,906,231-146,031,760 ABCE1, ANAPC10, 1 more genes
    nsv6741434copy number variation1nstd229human GRCh38 chr4: 144,943,417-145,127,593 , GRCh37.p13 chr4: 145,864,569-146,048,745 ABCE1, RN7SKP235, 1 more genes
    nsv6567247inversion1nstd223human GRCh38 chr4: 144,681,818-145,112,610 , GRCh37.p13 chr4: 145,602,970-146,033,762 ABCE1, ANAPC10, 3 more genes
    nsv6389300copy number variation1nstd223human GRCh38 chr4: 145,113,698-145,114,332 , GRCh37.p13 chr4: 146,034,850-146,035,484 ABCE1
    nsv6389066copy number variation1nstd223human GRCh38 chr4: 145,101,579-145,101,740 , GRCh37.p13 chr4: 146,022,731-146,022,892 ABCE1
    nsv6388384copy number variation1nstd223human GRCh38 chr4: 145,118,145-145,118,934 , GRCh37.p13 chr4: 146,039,297-146,040,086 ABCE1
    nsv6387103copy number variation1nstd223human GRCh38 chr4: 145,114,593-145,115,424 , GRCh37.p13 chr4: 146,035,745-146,036,576 ABCE1
    nsv6379556copy number variation1nstd223human GRCh38 chr4: 145,107,250-145,107,445 , GRCh37.p13 chr4: 146,028,402-146,028,597 ABCE1
    nsv6378471copy number variation1nstd223human GRCh38 chr4: 140,215,978-145,835,229 , GRCh37.p13 chr4: 141,137,132-146,756,381 OTUD4, GYPA, 62 more genes
    nsv6255459mobile element insertion1nstd215human GRCh38 chr4: 145,112,196-145,112,196 , GRCh37.p13 chr4: 146,033,348-146,033,348 ABCE1
    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
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5377674translocation1nstd200human GRCh38 chr4: 144,156,636-144,156,636 , GRCh38 chr4: 145,128,645-145,128,645 , GRCh37.p13 chr4: 146,049,797-146,049,797 , GRCh37.p13 chr4: 145,077,789-145,077,789 , ABCE1
    nsv5353235translocation1nstd200human GRCh38 chr4: 145,115,318-145,115,318 , GRCh38 chr4: 145,114,574-145,114,574 , GRCh37.p13 chr4: 146,036,470-146,036,470 , GRCh37.p13 chr4: 146,035,726-146,035,726 ABCE1
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