U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 117

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5528042copy number variation1nstd206human GRCh38 chr19: 33,303,714-33,304,146 , GRCh37.p13 chr19: 33,794,620-33,795,052 CEBPA-DT
    nsv5381195copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,532,300-33,793,320 , GRCh38.p12 chr19: 33,041,394-33,302,414 CEBPA-DT, WDR88, 6 more genes
    nsv5359729translocation1nstd200human GRCh38 chr19: 33,304,146-33,304,146 , GRCh38 chr19: 33,303,714-33,303,714 , GRCh37.p13 chr19: 33,795,052-33,795,052 , GRCh37.p13 chr19: 33,794,620-33,794,620 CEBPA-DT
    nsv4861273copy number variation1nstd200human GRCh37 chr19: 33,794,620-33,795,052 , GRCh38.p12 chr19: 33,303,714-33,304,146 CEBPA-DT
    nsv4684188copy number variation1nstd102humanPathogenic GRCh37 chr19: 33,792,329-33,792,330 , GRCh38 chr19: 33,301,423-33,301,424 CEBPA, CEBPA-DT
    nsv4578541copy number variation1nstd102humanPathogenic GRCh37 chr19: 33,792,369-33,792,370 , GRCh38 chr19: 33,301,463-33,301,464 CEBPA, CEBPA-DT
    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
    nsv4457363copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,688,375-33,831,558 , GRCh38.p12 chr19: 33,197,469-33,340,652 RPS3AP50, LRP3, 3 more genes
    nsv4454289copy number variation1nstd102humanUncertain significance GRCh38 chr19: 33,301,328-33,302,424 , GRCh37 chr19: 33,792,234-33,793,330 CEBPA-DT, CEBPA
    nsv4272271copy number variation1nstd166human GRCh37.p13 chr19: 33,794,620-33,795,052 , GRCh38.p12 chr19: 33,303,714-33,304,146 CEBPA-DT
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 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
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 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
    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
    nsv3900139copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494 ZNF599, FAM187B2P, 130 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center