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 216

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5284613copy number variation1nstd204human GRCh38.p13 chr19: 1,402,101-1,628,800 , GRCh37.p13 chr19: 1,402,100-1,628,799 TCF3, RN7SL477P, 13 more genes
    nsv5019054copy number variation1nstd200human GRCh38 chr19: 1,440,873-1,444,938 , GRCh37.p13 chr19: 1,440,872-1,444,937 RPS15, APC2
    nsv4868110copy number variation1nstd200human GRCh37 chr19: 1,440,872-1,444,937 , GRCh38.p12 chr19: 1,440,873-1,444,938 APC2, RPS15
    nsv4676366copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,075,192-2,256,387 , GRCh38.p12 chr19: 1,075,193-2,256,388 AMH, ATP5F1D, 64 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4457632copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,342,624-1,817,866 , GRCh38.p12 chr19: 1,342,625-1,817,867 ONECUT3, UQCR11, 23 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4267210copy number variation1nstd166human GRCh37.p13 chr19: 1,440,872-1,444,937 , GRCh38.p12 chr19: 1,440,873-1,444,938 APC2, RPS15
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
    nsv3922550copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-1,952,650 , GRCh37 chr19: 259,395-1,952,649 , NCBI36 chr19: 210,395-1,903,649 LOC102723811, DAZAP1, 99 more genes
    nsv3922151copy number variation1nstd102humanPathogenic NCBI36 chr19: 896,098-1,923,298 , GRCh38 chr19: 945,098-1,972,299 , GRCh37 chr19: 945,098-1,972,298 MIR1909, SBNO2, 58 more genes
    nsv3921932copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,506,147 , GRCh37 chr19: 259,395-2,555,147 , GRCh38 chr19: 259,395-2,555,149 GZMM, MIER2, 129 more genes
    nsv3920078copy number variation1nstd102humanUncertain significance GRCh38 chr19: 1,351,163-2,555,149 , NCBI36 chr19: 1,302,162-2,506,147 , GRCh37 chr19: 1,351,162-2,555,147 MKNK2, LOC101928543, 61 more genes
    nsv3918029copy number variation1nstd102humanPathogenic NCBI36 chr19: 226,925-1,843,275 , GRCh37 chr19: 275,925-1,892,275 , GRCh38 chr19: 275,925-1,892,276 GPX4, RPS2P52, 94 more genes
    nsv3913283copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 372,537-2,848,919 , GRCh37 chr19: 421,537-2,897,919 , GRCh38 chr19: 421,537-2,897,921 AMH, ATP5F1D, 135 more genes
    nsv3910990copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-2,068,507 , NCBI36 chr19: 210,395-2,019,506 , GRCh37 chr19: 259,395-2,068,506 SPMAP2, PTBP1, 102 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