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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943303copy number variation1nstd209human GRCh38 chr19: 35,905,860-35,911,124 , GRCh37.p13 chr19: 36,396,762-36,402,026 TYROBP
    nsv5885354copy number variation2nstd209human GRCh38 chr19: 35,907,609-35,908,880 , GRCh37.p13 chr19: 36,398,511-36,399,782 TYROBP
    nsv5883197copy number variation1nstd209human GRCh38 chr19: 35,905,909-35,910,380 , GRCh37.p13 chr19: 36,396,811-36,401,282 TYROBP
    nsv5869465copy number variation1nstd209human GRCh38 chr19: 35,906,009-35,907,108 , GRCh37.p13 chr19: 36,396,911-36,398,010 TYROBP
    nsv5672902copy number variation1nstd102humannot provided GRCh37 chr19: 36,396,785-36,402,026 , GRCh38 chr19: 35,905,883-35,911,124 TYROBP
    nsv5293162copy number variation1nstd204human GRCh38.p13 chr19: 35,905,501-35,908,600 , GRCh37.p13 chr19: 36,396,403-36,399,502 TYROBP
    nsv5285254copy number variation1nstd204human GRCh38.p13 chr19: 35,905,884-35,911,330 , GRCh37.p13 chr19: 36,396,786-36,402,232 TYROBP
    nsv5283949copy number variation1nstd204human GRCh38.p13 chr19: 35,897,401-35,905,500 , GRCh37.p13 chr19: 36,388,303-36,396,402 TYROBP, HCST, 1 more genes
    nsv5283289copy number variation1nstd204human GRCh38.p13 chr19: 35,908,581-35,909,580 , GRCh37.p13 chr19: 36,399,483-36,400,482 TYROBP
    nsv5194990mobile element insertion1nstd203human GRCh38 chr19: 35,904,144-35,904,160 , GRCh37.p13 chr19: 36,395,046-36,395,062 HCST, TYROBP
    nsv5176236mobile element insertion1nstd203human GRCh38 chr19: 35,905,623-35,905,652 , GRCh37.p13 chr19: 36,396,525-36,396,554 TYROBP
    nsv5027716copy number variation1nstd200human GRCh38 chr19: 35,905,921-35,911,089 , GRCh37.p13 chr19: 36,396,823-36,401,991 TYROBP
    nsv5024572copy number variation1nstd200human GRCh38 chr19: 35,818,267-36,019,433 , GRCh37.p13 chr19: 36,309,169-36,510,335 SYNE4, LOC107985317, 13 more genes
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4536962copy number variation1nstd166human GRCh37.p13 chr19: 36,309,999-36,510,300 , GRCh38.p12 chr19: 35,819,097-36,019,398 KIRREL2, HCST, 13 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
    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
    nsv4260287copy number variation1nstd166human GRCh37.p13 chr19: 36,386,986-36,397,669 , GRCh38.p12 chr19: 35,896,084-35,906,767 NFKBID, HCST, 1 more genes
    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
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