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 217

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146584insertion1nstd232human GRCh37.p13 chr19: 35,413,913-35,413,913 , GRCh38.p12 chr19: 34,923,009-34,923,009 ZNF30, ZNF30-AS1
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7016145copy number variation1nstd229human GRCh38 chr19: 34,877,770-34,940,187 , GRCh37.p13 chr19: 35,368,674-35,431,091 , ZNF30, 3 more genes
    nsv7008131copy number variation1nstd229human GRCh38 chr19: 34,932,578-34,935,426 , GRCh37.p13 chr19: 35,423,482-35,426,330 ZNF30
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7004980copy number variation1nstd229human GRCh38 chr19: 34,938,074-34,955,527 , GRCh37.p13 chr19: 35,428,978-35,446,431 ZNF792, ZNF30
    nsv7004402copy number variation1nstd229human GRCh38 chr19: 34,927,781-34,930,956 , GRCh37.p13 chr19: 35,418,685-35,421,860 ZNF30
    nsv7003962copy number variation1nstd229human GRCh38 chr19: 34,929,792-34,929,940 , GRCh37.p13 chr19: 35,420,696-35,420,844 ZNF30
    nsv7002769copy number variation1nstd229human GRCh38 chr19: 34,923,725-34,929,540 , GRCh37.p13 chr19: 35,414,629-35,420,444 ZNF30, ZNF30-AS1
    nsv7001269copy number variation1nstd229human GRCh38 chr19: 34,925,096-34,933,063 , GRCh37.p13 chr19: 35,416,000-35,423,967 ZNF30-AS1, ZNF30
    nsv7000202copy number variation1nstd229human GRCh38 chr19: 34,937,224-34,995,343 , GRCh37.p13 chr19: 35,428,128-35,486,247 GRAMD1A, ZNF30, 1 more genes
    nsv6600032inversion1nstd223human GRCh38 chr19: 34,932,786-34,933,459 , GRCh37.p13 chr19: 35,423,690-35,424,363 ZNF30
    nsv6598364inversion1nstd223human GRCh38 chr19: 34,940,631-34,941,468 , GRCh37.p13 chr19: 35,431,535-35,432,372 ZNF30
    nsv6598040inversion1nstd223human GRCh38 chr19: 34,936,807-34,937,083 , GRCh37.p13 chr19: 35,427,711-35,427,987 ZNF30
    nsv6520152copy number variation1nstd223human GRCh38 chr19: 34,923,077-34,923,121 , GRCh37.p13 chr19: 35,413,981-35,414,025 ZNF30, ZNF30-AS1
    nsv6516715copy number variation1nstd223human GRCh38 chr19: 34,937,224-34,995,343 , GRCh37.p13 chr19: 35,428,128-35,486,247 ZNF792, GRAMD1A, 1 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6251013mobile element insertion1nstd215human GRCh38 chr19: 34,935,726-34,935,726 , GRCh37.p13 chr19: 35,426,630-35,426,630 ZNF30
    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