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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138656copy number variation1nstd232human GRCh37.p13 chr19: 2,427,322-2,427,410 , GRCh38.p12 chr19: 2,427,324-2,427,412 TIMM13, LMNB2
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095644copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,456,055-2,456,931 , GRCh38.p12 chr19: 1,456,056-2,456,933 APC2, CSNK1G2, 49 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
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7064975inversion1nstd229human GRCh38 chr19: 2,409,662-2,423,767 , GRCh37.p13 chr19: 2,409,660-2,423,765 TIMM13, TMPRSS9
    nsv6637269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,376,834-2,515,283 , GRCh38.p12 chr19: 2,376,836-2,515,285 LINC01775, GNG7, 6 more genes
    nsv6624851copy number variation1nstd224human GRCh37 chr19: 2,374,093-2,487,858 , GRCh38.p12 chr19: 2,374,095-2,487,860 GADD45B, TIMM13, 4 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6596539inversion1nstd223human GRCh38 chr19: 2,409,662-2,423,767 , GRCh37.p13 chr19: 2,409,660-2,423,765 TMPRSS9, TIMM13
    nsv6534380copy number variation1nstd223human GRCh38 chr19: 2,379,318-2,594,919 , GRCh37.p13 chr19: 2,379,316-2,594,917 TMPRSS9, LMNB2, 8 more genes
    nsv6534128copy number variation1nstd223human GRCh38 chr19: 2,420,314-2,425,317 , GRCh37.p13 chr19: 2,420,312-2,425,315 TMPRSS9, TIMM13
    nsv6516546copy number variation1nstd223human GRCh38 chr19: 2,425,701-2,428,200 , GRCh37.p13 chr19: 2,425,699-2,428,198 LMNB2, TMPRSS9, 1 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
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5561268sequence alteration1nstd206human GRCh38 chr19: 2,409,661-2,423,767 , GRCh37.p13 chr19: 2,409,659-2,423,765 TIMM13, TMPRSS9
    nsv5292953copy number variation1nstd204human GRCh38.p13 chr19: 2,349,101-2,713,600 , GRCh37.p13 chr19: 2,349,099-2,713,598 TMPRSS9, RNU6-993P, 11 more genes
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv4684376copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,273,150-2,897,133 , GRCh38.p12 chr19: 2,273,151-2,897,135 LOC101928572, TIMM13, 24 more genes
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