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 98

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093322copy number variation1nstd102humanUncertain significance GRCh38 chr19: 46,411,762-46,411,833 , GRCh37 chr19: 46,915,019-46,915,090 CCDC8
    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
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 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
    nsv7013675copy number variation1nstd229human GRCh38 chr19: 46,397,377-46,422,269 , GRCh37.p13 chr19: 46,900,634-46,925,526 LOC105372426, CCDC8
    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
    nsv7007469copy number variation1nstd229human GRCh38 chr19: 46,406,701-46,420,011 , GRCh37.p13 chr19: 46,909,958-46,923,268 CCDC8
    nsv7001243copy number variation1nstd229human GRCh38 chr19: 46,284,776-46,513,348 , GRCh37.p13 chr19: 46,788,033-47,016,605 RNU6-924P, HIF3A, 6 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
    nsv6310454copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,914,947-46,915,018 , GRCh38 chr19: 46,411,690-46,411,761 CCDC8
    nsv6310435copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,914,889-46,914,890 , GRCh38 chr19: 46,411,632-46,411,633 CCDC8
    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
    nsv6103268inversion1nstd212human GRCh38 chr19: 45,080,087-46,509,008 , GRCh37.p13 chr19: 45,583,345-47,012,265 , CKM, 72 more genes
    nsv4680491copy number variation1nstd189human GRCh37.p13 chr19: 46,787,206-47,086,561 , GRCh38.p12 chr19: 46,283,949-46,583,304 , PPP5C, 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
    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
    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