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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5698986mobile element insertion1nstd211human GRCh38 chr19: 35,522,740-35,522,740 , GRCh37.p13 chr19: 36,013,642-36,013,642 SBSN
    nsv5652418insertion1nstd207human GRCh38 chr19: 35,527,213-35,527,213 , GRCh37.p13 chr19: 36,018,115-36,018,115 SBSN
    nsv5597427copy number variation1nstd207human GRCh38 chr19: 35,527,667-35,527,720 , GRCh37.p13 chr19: 36,018,569-36,018,622 SBSN
    nsv5515830copy number variation1nstd206human GRCh38 chr19: 35,527,256-35,528,837 , GRCh37.p13 chr19: 36,018,158-36,019,739 SBSN
    nsv5415494mobile element insertion1nstd206human GRCh38 chr19: 35,522,740-35,522,791 , GRCh37.p13 chr19: 36,013,642-36,013,693 SBSN
    nsv5027696copy number variation1nstd200human GRCh38 chr19: 35,525,038-35,527,876 , GRCh37.p13 chr19: 36,015,940-36,018,778 SBSN
    nsv5027695copy number variation1nstd200human GRCh38 chr19: 35,520,134-35,521,736 , GRCh37.p13 chr19: 36,011,036-36,012,638 SBSN
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4625709copy number variation2nstd183human GRCh37 chr19: 36,018,030-36,019,735 , GRCh38.p12 chr19: 35,527,128-35,528,833 SBSN
    nsv4535903copy number variation1nstd166human GRCh37.p13 chr19: 36,018,078-36,018,545 , GRCh38.p12 chr19: 35,527,176-35,527,643 SBSN
    nsv4499678mobile element insertion1nstd166human GRCh37.p13 chr19: 36,013,628-36,013,628 , GRCh38.p12 chr19: 35,522,726-35,522,726 SBSN
    nsv4457800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984 SBSN, UPK1A, 38 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4441761insertion1nstd175human GRCh37 chr19: 36,018,002-36,018,002 , GRCh38.p12 chr19: 35,527,100-35,527,100 SBSN
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4264115copy number variation1nstd166human GRCh37.p13 chr19: 36,011,036-36,012,638 , GRCh38.p12 chr19: 35,520,134-35,521,736 SBSN
    nsv3943744insertion1nstd167human GRCh37 chr19: 36,018,115-36,018,115 , GRCh38.p12 chr19: 35,527,213-35,527,213 SBSN
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
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