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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147870copy number variation1nstd232human GRCh37.p13 chr19: 4,494,051-4,494,158 , GRCh38.p12 chr19: 4,494,054-4,494,161 HDGFL2
    nsv7141156insertion1nstd232human GRCh37.p13 chr19: 4,496,404-4,496,404 , GRCh38.p12 chr19: 4,496,407-4,496,407 HDGFL2
    nsv7140619copy number variation1nstd232human GRCh37.p13 chr19: 4,491,675-4,491,755 , GRCh38.p12 chr19: 4,491,678-4,491,758 HDGFL2
    nsv7139022copy number variation1nstd232human GRCh37.p13 chr19: 4,475,348-4,475,440 , GRCh38.p12 chr19: 4,475,351-4,475,443 HDGFL2
    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
    nsv7016144copy number variation1nstd229human GRCh38 chr19: 4,484,978-4,487,919 , GRCh37.p13 chr19: 4,484,975-4,487,916 HDGFL2
    nsv7013774copy number variation1nstd229human GRCh38 chr19: 4,497,442-4,532,495 , GRCh37.p13 chr19: 4,497,439-4,532,507 PLIN4, PLIN5, 1 more genes
    nsv7008007copy number variation1nstd229human GRCh38 chr19: 4,481,615-4,487,547 , GRCh37.p13 chr19: 4,481,612-4,487,544 HDGFL2
    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
    nsv6533493copy number variation1nstd223human GRCh38 chr19: 4,492,833-4,493,295 , GRCh37.p13 chr19: 4,492,830-4,493,292 HDGFL2
    nsv6520323copy number variation1nstd223human GRCh38 chr19: 4,463,447-4,470,307 , GRCh37.p13 chr19: 4,463,444-4,470,304 HDGFL2
    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
    nsv6242755mobile element insertion1nstd215human GRCh38 chr19: 4,495,559-4,495,559 , GRCh37.p13 chr19: 4,495,556-4,495,556 HDGFL2
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