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 115

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929723copy number variation1nstd209human GRCh38 chr19: 47,747,950-47,748,094 , GRCh37.p13 chr19: 48,251,207-48,251,351 NOP53
    nsv5880325copy number variation1nstd209human GRCh38 chr19: 47,752,521-47,753,820 , GRCh37.p13 chr19: 48,255,778-48,257,077 NOP53
    nsv5870103copy number variation1nstd209human GRCh38 chr19: 47,751,021-47,752,320 , GRCh37.p13 chr19: 48,254,278-48,255,577 NOP53
    nsv5525532copy number variation1nstd206human GRCh38 chr19: 47,744,354-47,744,737 , GRCh37.p13 chr19: 48,247,611-48,247,994 NOP53
    nsv5321019copy number variation1nstd204human GRCh38.p13 chr19: 47,744,324-47,744,766 , GRCh37.p13 chr19: 48,247,581-48,248,023 NOP53
    nsv5024771copy number variation1nstd200human GRCh38 chr19: 47,753,175-47,754,044 , GRCh37.p13 chr19: 48,256,432-48,257,301 NOP53, SNORD23
    nsv5020856copy number variation1nstd200human GRCh38 chr19: 47,749,087-47,755,288 , GRCh37.p13 chr19: 48,252,344-48,258,545 SNORD23, NOP53, 1 more genes
    nsv4853213copy number variation1nstd200human GRCh37 chr19: 48,252,344-48,258,545 , GRCh38.p12 chr19: 47,749,087-47,755,288 NOP53-AS1, NOP53, 1 more genes
    nsv4853212copy number variation1nstd200human GRCh37 chr19: 48,247,611-48,247,994 , GRCh38.p12 chr19: 47,744,354-47,744,737 NOP53
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4679541copy number variation1nstd189human GRCh37.p13 chr19: 48,085,948-48,392,233 , GRCh38.p12 chr19: 47,582,691-47,888,976 CRX, SELENOW, 10 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676184copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,043,102-48,402,210 , GRCh38.p12 chr19: 47,539,845-47,898,953 RPL23AP80, SULT2A1, 12 more genes
    nsv4625283copy number variation1nstd183human GRCh37 chr19: 48,214,990-48,290,706 , GRCh38.p12 chr19: 47,711,733-47,787,449 NOP53-AS1, SELENOW, 3 more genes
    nsv4457853copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699 DHDH, GRIN2D, 94 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
    nsv4428461copy number variation1nstd174human GRCh37 chr19: 48,250,461-48,411,104 , GRCh38.p12 chr19: 47,747,204-47,907,847 RPL23AP80, SNAR-A12, 9 more genes
    nsv4350827copy number variation1nstd102humanPathogenic GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279 LINC01595, SNAR-A13, 59 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4261951copy number variation1nstd166human GRCh37.p13 chr19: 48,247,611-48,247,994 , GRCh38.p12 chr19: 47,744,354-47,744,737 NOP53
    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