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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7098146copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,478,774-98,779,708 , GRCh38.p12 chr7: 98,881,151-99,182,085 SMURF1, MIR3609, 5 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv6837146copy number variation1nstd229human GRCh38 chr7: 99,034,776-99,034,870 , GRCh37.p13 chr7: 98,632,399-98,632,493 LOC101927550, SMURF1
    nsv6828132copy number variation1nstd229human GRCh38 chr7: 98,667,290-99,135,243 , GRCh37.p13 chr7: 98,296,602-98,556,215 , GRCh37.p13 chr7|NW_003571041.1: 36,472-327,774 SMURF1, TRRAP, 7 more genes
    nsv6826605copy number variation1nstd229human GRCh38 chr7: 99,017,564-99,021,463 , GRCh37.p13 chr7: 98,615,187-98,619,086 LOC101927550
    nsv6823136copy number variation1nstd229human GRCh38 chr7: 99,031,994-99,287,914 , GRCh37.p13 chr7: 98,629,617-98,885,537 LOC105375421, MYH16, 3 more genes
    nsv6822030copy number variation1nstd229human GRCh38 chr7: 98,865,322-99,195,183 , GRCh37.p13 chr7: 98,556,216-98,792,806 TMEM130, SCARNA28, 6 more genes
    nsv6819827copy number variation1nstd229human GRCh38 chr7: 98,885,199-99,094,341 , GRCh37.p13 chr7: 98,556,216-98,691,964 TRRAP, RNF14P3, 2 more genes
    nsv6818787copy number variation1nstd229human GRCh38 chr7: 99,030,928-99,038,777 , GRCh37.p13 chr7: 98,628,551-98,636,400 SMURF1, LOC101927550
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6618228copy number variation1nstd223human GRCh38 chr7: 99,008,093-99,022,874 , GRCh37.p13 chr7: 98,605,716-98,620,497 LOC101927550, TRRAP
    nsv6616739copy number variation1nstd223human GRCh38 chr7: 98,806,653-99,083,746 , GRCh37.p13 chr7|NW_003571041.1: 175,835-327,774 , GRCh37.p13 chr7: 98,404,276-98,556,215 SMURF1, TMEM130, 5 more genes
    nsv6609359copy number variation1nstd223human GRCh38 chr7: 99,027,119-99,036,428 , GRCh37.p13 chr7: 98,624,742-98,634,051 SMURF1, LOC101927550
    nsv6601472copy number variation1nstd223human GRCh38 chr7: 99,017,561-99,021,465 , GRCh37.p13 chr7: 98,615,184-98,619,088 LOC101927550
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6142335copy number variation1nstd206human GRCh38 chr7: 99,027,079-99,036,471 , GRCh37.p13 chr7: 98,624,702-98,634,094 LOC101927550, SMURF1
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
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