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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705278mobile element insertion1nstd211human GRCh38 chr13: 18,912,717-18,912,717 , GRCh37.p13 chr13: 19,486,857-19,486,857 LINC00408
    nsv5700772mobile element insertion1nstd211human GRCh38 chr13: 18,921,169-18,921,169 , GRCh37.p13 chr13: 19,495,309-19,495,309 LINC00408
    nsv5657524insertion1nstd207human GRCh38 chr13: 18,904,351-18,904,351 , GRCh37.p13 chr13: 19,478,491-19,478,491 LINC00408
    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
    nsv5422668mobile element insertion1nstd206human GRCh38 chr13: 18,912,717-18,912,765 , GRCh37.p13 chr13: 19,486,857-19,486,905 LINC00408
    nsv5421836mobile element insertion1nstd206human GRCh38 chr13: 18,921,169-18,921,220 , GRCh37.p13 chr13: 19,495,309-19,495,360 LINC00408
    nsv4996375copy number variation1nstd200human GRCh38 chr13: 18,904,248-18,904,327 , GRCh37.p13 chr13: 19,478,388-19,478,467 LINC00408
    nsv4996373copy number variation1nstd200human GRCh38 chr13: 18,888,235-19,103,184 , GRCh37.p13 chr13: 19,462,375-19,677,324 PHF2P1, LINC00442, 7 more genes
    nsv4675707copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,436,286-20,886,867 , GRCh38.p12 chr13: 18,862,146-20,312,728 PHF2P1, MRPL3P1, 43 more genes
    nsv4675550copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223 MRPL57, TATDN2P3, 129 more genes
    nsv4616752copy number variation2nstd183human GRCh37 chr13: 19,405,750-19,596,825 , GRCh38.p12 chr13: 18,850,545-19,022,685 ANKRD20A9P, LINC00442, 6 more genes
    nsv4607228copy number variation2nstd183human GRCh37 chr13: 19,037,783-19,499,149 , GRCh38.p12 chr13: 18,463,643-18,925,009 VN1R58P, ANKRD20A9P, 18 more genes
    nsv4603544copy number variation1nstd183human GRCh37 chr13: 19,477,595-19,479,188 , GRCh38.p12 chr13: 18,903,455-18,905,048 LINC00408
    nsv4506529mobile element insertion1nstd166human GRCh37.p13 chr13: 19,482,013-19,482,013 , GRCh38.p12 chr13: 18,907,873-18,907,873 LINC00408
    nsv4455063copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-23,274,540 , GRCh38.p12 chr13: 18,862,146-22,700,401 SAP18, LOC105370102, 90 more genes
    nsv4421946copy number variation1nstd174human GRCh37 chr13: 19,026,949-19,527,891 , GRCh38.p12 chr13: 18,452,809-18,953,751 CNN2P12, ANKRD20A9P, 19 more genes
    nsv4368390copy number variation1nstd173human GRCh37 chr13: 19,436,287-19,605,397 , GRCh38.p12 chr13: 18,862,147-19,031,257 ANKRD20A9P, LINC00442, 7 more genes
    nsv4214889copy number variation1nstd166human GRCh37.p13 chr13: 19,492,618-19,697,373 , GRCh38.p12 chr13: 18,918,478-19,123,233 PHF2P1, LINC00442, 6 more genes
    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
    nsv3919574copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,850,545-114,327,173 , GRCh37 chr13: 19,296,527-115,085,141 , NCBI36 chr13: 18,194,527-114,110,750 RNU6-77P, LINC00457, 1317 more genes
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