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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143507copy number variation1nstd232human GRCh38.p12 chr19: 4,446,411-4,446,496 , GRCh37.p13 chr19: 4,446,408-4,446,493 CHAF1A, UBXN6, 1 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7017810copy number variation1nstd229human GRCh38 chr19: 4,323,001-4,523,900 , GRCh37.p13 chr19: 4,322,998-4,523,912 CHAF1A, FSD1, 9 more genes
    nsv7012058copy number variation1nstd229human GRCh38 chr19: 4,434,220-4,434,728 , GRCh37.p13 chr19: 4,434,217-4,434,725 CHAF1A
    nsv7003449copy number variation1nstd229human GRCh38 chr19: 4,417,392-4,452,994 , GRCh37.p13 chr19: 4,417,389-4,452,991 UBXN6, MIR4746, 1 more genes
    nsv6634858copy number variation1nstd227human GRCh38.p12 chr19: 4,340,745-4,575,361 , GRCh37 chr19: 4,340,742-4,575,373 SH3GL1, CHAF1A, 10 more genes
    nsv6598603inversion1nstd223human GRCh38 chr19: 4,262,367-4,610,905 , GRCh37.p13 chr19: 4,262,364-4,610,917 STAP2, FSD1, 15 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6534771copy number variation1nstd223human GRCh38 chr19: 4,418,997-4,419,493 , GRCh37.p13 chr19: 4,418,994-4,419,490 CHAF1A
    nsv6530296copy number variation1nstd223human GRCh38 chr19: 4,447,469-4,452,083 , GRCh37.p13 chr19: 4,447,466-4,452,080 UBXN6, CHAF1A
    nsv6523923copy number variation1nstd223human GRCh38 chr19: 4,419,859-4,421,315 , GRCh37.p13 chr19: 4,419,856-4,421,312 CHAF1A
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 RN7SL202P, EIF1P6, 67 more genes
    nsv6291557copy number variation1nstd102humanUncertain significance GRCh37 chr19: 4,182,912-4,633,772 , GRCh38.p12 chr19: 4,182,915-4,633,760 STAP2, MIR4746, 19 more genes
    nsv6145261copy number variation1nstd206human GRCh38 chr19: 4,344,000-4,468,000 , GRCh37.p13 chr19: 4,343,997-4,467,997 , SH3GL1, 5 more genes
    nsv6144729copy number variation1nstd206human GRCh38 chr19: 4,410,000-4,420,000 , GRCh37.p13 chr19: 4,409,997-4,419,997 , CHAF1A
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
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