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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097363copy number variation2nstd102humanPathogenic GRCh37 chr7: 20,994,491-23,030,730 , GRCh38.p12 chr7: 20,954,872-22,991,111 STEAP1B-AS1, RNA5SP227, 25 more genes
    nsv7057183inversion1nstd229human GRCh38 chr7: 21,972,222-23,503,741 , GRCh37.p13 chr7: 22,011,840-23,543,360 TRA2A, IGF2BP3, 30 more genes
    nsv7048269inversion1nstd229human GRCh38 chr7: 22,481,392-22,816,505 , GRCh37.p13 chr7: 22,521,011-22,856,124 RPS26P32, STEAP1B-AS1, 7 more genes
    nsv6807963copy number variation1nstd229human GRCh38 chr7: 22,420,277-22,752,629 , GRCh37.p13 chr7: 22,459,896-22,792,248 STEAP1B, STEAP1B-AS1, 5 more genes
    nsv6806790copy number variation1nstd229human GRCh38 chr7: 22,724,584-22,749,673 , GRCh37.p13 chr7: 22,764,203-22,789,292 IL6, IL6-AS1, 1 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631686copy number variation1nstd224human GRCh37 chr7: 22,712,877-23,240,353 , GRCh38.p12 chr7: 22,673,258-23,200,734 TOMM7, RPS26P32, 15 more genes
    nsv6618986copy number variation1nstd223human GRCh38 chr7: 22,732,101-22,734,300 , GRCh37.p13 chr7: 22,771,720-22,773,919 IL6
    nsv6573963inversion1nstd223human GRCh38 chr7: 22,481,389-22,816,508 , GRCh37.p13 chr7: 22,521,008-22,856,127 IL6, TOMM7, 7 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6312441copy number variation1nstd102humanUncertain significance GRCh37 chr7: 20,994,491-23,213,917 , GRCh38.p12 chr7: 20,954,872-23,174,298 IL6, LOC105375186, 30 more genes
    nsv6278764insertion1nstd214human GRCh38 chr7: 22,732,256-22,732,256 , GRCh37.p13 chr7: 22,771,875-22,771,875 IL6
    nsv6135987copy number variation1nstd213human GRCh37 chr7: 22,640,000-23,010,001 , GRCh38.p12 chr7: 22,600,381-22,970,382 IL6, HYCC1, 10 more genes
    nsv6135755copy number variation1nstd213human GRCh37 chr7: 22,230,000-24,400,001 , GRCh38.p12 chr7: 22,190,382-24,360,382 IL6, RAPGEF5, 43 more genes
    nsv6075213insertion1nstd212human GRCh38 chr7: 22,732,258-22,732,258 , GRCh37.p13 chr7: 22,771,877-22,771,877 IL6
    nsv6075045insertion1nstd212human GRCh38 chr7: 22,732,307-22,732,307 , GRCh37.p13 chr7: 22,771,926-22,771,926 IL6
    nsv5679400mobile element insertion1nstd211human GRCh38 chr7: 22,729,198-22,729,198 , GRCh37.p13 chr7: 22,768,817-22,768,817 IL6
    nsv5631511insertion1nstd207human GRCh38 chr7: 22,732,256-22,732,256 , GRCh37.p13 chr7: 22,771,875-22,771,875 IL6
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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