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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5660874insertion1nstd207human GRCh38 chr19: 35,350,843-35,350,843 , GRCh37.p13 chr19: 35,841,746-35,841,746 FFAR1
    nsv5027689copy number variation1nstd200human GRCh38 chr19: 35,350,576-35,363,378 , GRCh37.p13 chr19: 35,841,479-35,854,280 FFAR3, FFAR1
    nsv5024563copy number variation1nstd200human GRCh38 chr19: 35,349,764-35,362,435 , GRCh37.p13 chr19: 35,840,667-35,853,337 FFAR1, FFAR3
    nsv4868175copy number variation1nstd200human GRCh37 chr19: 35,841,444-35,854,076 , GRCh38.p12 chr19: 35,350,541-35,363,174 FFAR3, FFAR1
    nsv4676336copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,811,335-35,898,248 , GRCh38.p12 chr19: 35,320,432-35,407,346 EEF1A1P7, MIR5196, 5 more genes
    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
    nsv4633073copy number variation1nstd183human GRCh37 chr19: 35,811,336-35,861,848 , GRCh38.p12 chr19: 35,320,433-35,370,946 CD22, FFAR1, 3 more genes
    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
    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
    nsv4258570copy number variation1nstd166human GRCh37.p13 chr19: 35,842,000-35,854,000 , GRCh38.p12 chr19: 35,351,097-35,363,098 FFAR1, FFAR3
    nsv3966092copy number variation1nstd168human GRCh38 chr19: 35,349,010-35,383,808 , GRCh37.p13 chr19: 35,839,913-35,874,710 FFAR1, EEF1A1P7, 2 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
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 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
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3906538copy number variation1nstd102humanBenign GRCh37 chr19: 35,658,728-36,173,537 , GRCh38.p12 chr19: 35,167,825-35,682,635 ATP4A, UPK1A-AS1, 33 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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