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 99

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    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
    nsv5980120insertion1nstd209human GRCh38 chr19: 47,226,081-47,226,081 , GRCh37.p13 chr19: 47,729,338-47,729,338 BBC3, MIR3191, 1 more genes
    nsv5711346mobile element insertion1nstd211human GRCh38 chr19: 47,225,945-47,225,945 , GRCh37.p13 chr19: 47,729,202-47,729,202 BBC3, MIR3191, 1 more genes
    nsv5664469insertion1nstd207human GRCh38 chr19: 47,226,081-47,226,081 , GRCh37.p13 chr19: 47,729,338-47,729,338 BBC3, MIR3191, 1 more genes
    nsv5539433insertion1nstd206human GRCh38 chr19: 47,226,108-47,226,132 , GRCh37.p13 chr19: 47,729,365-47,729,389 BBC3, MIR3191, 1 more genes
    nsv5327131copy number variation1nstd204human GRCh37.p13 chr19: 47,728,583-47,728,870 , GRCh38.p13 chr19: 47,225,326-47,225,613 BBC3, MIR3191, 1 more genes
    nsv5293275copy number variation1nstd204human GRCh38.p13 chr19: 47,049,201-47,476,100 , GRCh37.p13 chr19: 47,552,459-47,979,357 , ZC3H4, 12 more genes
    nsv5287634copy number variation1nstd204human GRCh38.p13 chr19: 47,201,401-47,396,100 , GRCh37.p13 chr19: 47,704,658-47,899,357 , DHX34, 8 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
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4676254copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,331,662-48,234,260 , GRCh38.p12 chr19: 46,828,405-47,731,003 AP2S1, BICRA, 22 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