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 93

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    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
    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
    nsv4676347copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,469,730-51,916,485 , GRCh38.p12 chr19: 49,966,473-51,413,231 VRK3, SYT3, 93 more genes
    nsv4457465copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814 MED25, EMC10, 117 more genes
    nsv4388480copy number variation1nstd173human GRCh37 chr19: 51,321,391-51,348,924 , GRCh38.p12 chr19: 50,818,135-50,845,668 KLK15, KLK1, 2 more genes
    nsv4379351copy number variation123nstd173human GRCh37 chr19: 51,321,391-51,345,568 , GRCh38.p12 chr19: 50,818,135-50,842,312 LOC105372441, KLK1, 2 more genes
    nsv4377402copy number variation2nstd173human GRCh37 chr19: 51,320,925-51,345,568 , GRCh38.p12 chr19: 50,817,669-50,842,312 KLK1, LINC01869, 2 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
    nsv3964909copy number variation1nstd168human GRCh38 chr19: 50,822,400-50,832,290 , GRCh37.p13 chr19: 51,325,656-51,335,546 KLK1, KLK15, 1 more genes
    nsv3931563insertion1nstd167human GRCh37 chr19: 51,321,919-51,321,919 , GRCh38.p12 chr19: 50,818,663-50,818,663 KLK1, LINC01869
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 KCNA7, ZNF28, 697 more genes
    nsv3916611copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818 RNU6-980P, ERVV-1, 526 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 LOC107987270, MIR6799, 694 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
    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