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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5152670mobile element insertion1nstd203human GRCh38 chr13: 52,808,057-52,808,088 , GRCh37.p13 chr13: 53,382,192-53,382,223 MIR759
    nsv5145053mobile element insertion1nstd203human GRCh38 chr13: 52,808,070-52,808,074 , GRCh37.p13 chr13: 53,382,205-53,382,209 MIR759
    nsv5008695copy number variation1nstd200human GRCh38 chr13: 52,744,264-52,836,186 , GRCh37.p13 chr13: 53,318,399-53,410,321 PPIAP26, MIR759
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4769378copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,170,957-57,713,087 , GRCh38.p12 chr13: 51,596,821-57,138,953 CTAGE3P, TMEM272, 46 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4456820copy number variation1nstd102humanUncertain significance GRCh37 chr13: 49,586,017-61,311,845 , GRCh38.p12 chr13: 49,011,881-60,737,711 MIR759, CAB39L, 149 more genes
    nsv4228148copy number variation1nstd166human GRCh37.p13 chr13: 53,382,202-53,382,268 , GRCh38.p12 chr13: 52,808,067-52,808,133 MIR759
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
    nsv3923642copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,738,887-115,085,141 , NCBI36 chr13: 43,636,887-114,110,750 , GRCh38 chr13: 44,164,751-114,327,173 LOC107984554, HNRNPA1P18, 861 more genes
    nsv3922463copy number variation1nstd102humanPathogenic NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628 TULP3P1, LOC105370349, 1311 more genes
    nsv3921223copy number variation1nstd102humanPathogenic GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141 TRIM60P13, LINC00351, 1289 more genes
    nsv3920749copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,407,270-115,064,089 , GRCh38 chr13: 19,833,130-114,298,614 , NCBI36 chr13: 19,305,270-114,082,191 DIAPH3-AS2, LOC105370216, 1281 more genes
    nsv3920039copy number variation2nstd102humanPathogenic GRCh37 chr13: 31,937,609-91,227,546 , NCBI36 chr13: 30,835,609-90,025,547 , GRCh38 chr13: 31,363,472-90,575,292 PSMD10P3, CPB2, 714 more genes
    nsv3919899copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,955,694-55,067,489 , GRCh38 chr13: 52,381,559-54,493,354 , NCBI36 chr13: 51,853,695-53,965,490 HNRNPA1L2, MIR1297, 20 more genes
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