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 140

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148237copy number variation1nstd102humanUncertain significance GRCh38 chr19: 47,257,435-47,886,413 , GRCh37.p13 chr19: 47,760,692-48,389,670 KPTN, RPL23AP80, 22 more genes
    nsv7137151copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 47,028,919-48,185,409 , GRCh38.p12 chr19: 46,525,662-47,682,152 C5AR1, CALM3, 36 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7073220inversion1nstd229human GRCh38 chr19: 45,719,988-49,018,157 , GRCh37.p13 chr19: 46,223,246-49,521,414 RUVBL2, NTN5, 150 more genes
    nsv7072237inversion1nstd229human GRCh38 chr19: 47,047,927-47,435,103 , GRCh37.p13 chr19: 47,551,185-47,938,360 MIR3190, C5AR1, 11 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7012452copy number variation1nstd229human GRCh38 chr19: 45,998,776-48,954,957 , GRCh37.p13 chr19: 46,502,034-49,458,214 TMEM160, SNORD23, 131 more genes
    nsv7008580copy number variation1nstd229human GRCh38 chr19: 47,267,249-47,271,761 , GRCh37.p13 chr19: 47,770,506-47,775,018 CCDC9
    nsv7000591copy number variation1nstd229human GRCh38 chr19: 47,254,259-47,256,393 , GRCh37.p13 chr19: 47,757,516-47,759,650 CCDC9
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6530554copy number variation1nstd223human GRCh38 chr19: 47,254,542-47,255,812 , GRCh37.p13 chr19: 47,757,799-47,759,069 CCDC9
    nsv6528812copy number variation1nstd223human GRCh38 chr19: 47,269,465-47,270,083 , GRCh37.p13 chr19: 47,772,722-47,773,340 CCDC9
    nsv6518383copy number variation1nstd223human GRCh38 chr19: 47,264,361-47,266,492 , GRCh37.p13 chr19: 47,767,618-47,769,749 CCDC9
    nsv6517712copy number variation1nstd223human GRCh38 chr19: 47,254,259-47,256,389 , GRCh37.p13 chr19: 47,757,516-47,759,646 CCDC9
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv6047975copy number variation1nstd212human GRCh38 chr19: 47,262,286-47,262,436 , GRCh37.p13 chr19: 47,765,543-47,765,693 CCDC9
    nsv5947074copy number variation1nstd209human GRCh38 chr19: 47,255,238-47,255,533 , GRCh37.p13 chr19: 47,758,495-47,758,790 CCDC9
    nsv5939844copy number variation1nstd209human GRCh38 chr19: 47,255,811-47,256,100 , GRCh37.p13 chr19: 47,759,068-47,759,357 CCDC9
    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