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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
    nsv5027958copy number variation1nstd200human GRCh38 chr19: 39,647,226-39,728,092 , GRCh37.p13 chr19: 40,137,866-40,218,732 LGALS14, LGALS16, 2 more genes
    nsv5027957copy number variation1nstd200human GRCh38 chr19: 39,637,056-39,820,842 , GRCh37.p13 chr19: 40,127,696-40,311,482 CLC, LGALS14, 6 more genes
    nsv4868346copy number variation1nstd200human GRCh37 chr19: 40,137,866-40,218,732 , GRCh38.p12 chr19: 39,647,226-39,728,092 LGALS14, LGALS16, 2 more genes
    nsv4711068copy number variation1nstd195human GRCh37 chr19: 40,160,851-40,204,601 , GRCh38.p12 chr19: 39,670,211-39,713,961 LGALS14, LGALS17A, 1 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
    nsv4373090copy number variation1nstd173human GRCh37 chr19: 40,071,956-40,266,526 , GRCh38.p12 chr19: 39,581,316-39,775,886 LOC100129935, LGALS17A, 10 more genes
    nsv4264741copy number variation1nstd166human GRCh37.p13 chr19: 40,127,696-40,311,482 , GRCh38.p12 chr19: 39,637,056-39,820,842 CLC, LGALS14, 6 more genes
    nsv3962172insertion1nstd168human GRCh38 chr19: 39,692,707-39,703,092 , GRCh37.p13 chr19: 40,183,347-40,193,732 LGALS14, RPS29P27
    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
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3908738copy number variation1nstd102humanUncertain significance GRCh37 chr19: 40,194,966-40,276,461 , GRCh38.p12 chr19|NW_009646206.1: 1-45,697 , GRCh38.p12 chr19: 39,704,326-39,785,821 CLC, LGALS14, 1 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
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3890299copy number variation1nstd102humanLikely benign GRCh37 chr19: 40,129,200-40,216,211 , GRCh38.p12 chr19: 39,638,560-39,725,571 LGALS14, LGALS16, 4 more genes
    nsv3242497insertion1nstd152human GRCh38 chr19: 39,703,797-39,712,353 , GRCh37.p13 chr19: 40,194,437-40,202,993 LGALS14
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3167629copy number variation10nstd151human GRCh37 chr19: 40,196,545-40,228,597 , GRCh38.p12 chr19: 39,705,905-39,737,957 CLC, LGALS14
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