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 492

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7062398inversion1nstd229human GRCh38 chr8: 133,487,926-133,530,218 , GRCh37.p13 chr8: 134,500,169-134,542,461 ST3GAL1
    nsv6857386copy number variation1nstd229human GRCh38 chr8: 133,480,093-133,489,322 , GRCh37.p13 chr8: 134,492,336-134,501,565 ST3GAL1
    nsv6856834copy number variation1nstd229human GRCh38 chr8: 133,513,227-133,516,904 , GRCh37.p13 chr8: 134,525,470-134,529,147 ST3GAL1
    nsv6856681copy number variation1nstd229human GRCh38 chr8: 133,461,349-133,461,510 , GRCh37.p13 chr8: 134,473,592-134,473,753 ST3GAL1
    nsv6856220copy number variation1nstd229human GRCh38 chr8: 133,484,561-133,484,748 , GRCh37.p13 chr8: 134,496,804-134,496,991 ST3GAL1
    nsv6855193copy number variation1nstd229human GRCh38 chr8: 133,552,191-133,553,739 , GRCh37.p13 chr8: 134,564,434-134,565,982 ST3GAL1
    nsv6851025copy number variation1nstd229human GRCh38 chr8: 133,235,286-133,528,528 , GRCh37.p13 chr8: 134,247,529-134,540,771 ST3GAL1, ST13P6, 4 more genes
    nsv6849665copy number variation1nstd229human GRCh38 chr8: 133,542,517-133,546,788 , GRCh37.p13 chr8: 134,554,760-134,559,031 ST3GAL1
    nsv6849476copy number variation1nstd229human GRCh38 chr8: 133,535,283-133,570,139 , GRCh37.p13 chr8: 134,547,526-134,582,382 ST3GAL1
    nsv6847730copy number variation1nstd229human GRCh38 chr8: 133,441,401-133,588,300 , GRCh37.p13 chr8: 134,453,644-134,600,543 ST3GAL1
    nsv6846184copy number variation1nstd229human GRCh38 chr8: 133,515,618-133,519,156 , GRCh37.p13 chr8: 134,527,861-134,531,399 ST3GAL1
    nsv6844385copy number variation1nstd229human GRCh38 chr8: 132,809,731-133,525,064 , GRCh37.p13 chr8: 133,821,976-134,537,307 CCN4, ST13P6, 14 more genes
    nsv6844370copy number variation1nstd229human GRCh38 chr8: 133,517,585-133,523,201 , GRCh37.p13 chr8: 134,529,828-134,535,444 ST3GAL1
    nsv6841897copy number variation1nstd229human GRCh38 chr8: 133,476,201-133,482,900 , GRCh37.p13 chr8: 134,488,444-134,495,143 ST3GAL1
    nsv6841859copy number variation1nstd229human GRCh38 chr8: 133,452,454-133,583,185 , GRCh37.p13 chr8: 134,464,697-134,595,428 ST3GAL1
    nsv6841401copy number variation1nstd229human GRCh38 chr8: 133,010,316-136,879,429 , GRCh37.p13 chr8: 134,022,561-137,891,672 LOC107986978, LOC101927822, 35 more genes
    nsv6840734copy number variation1nstd229human GRCh38 chr8: 133,502,622-133,508,193 , GRCh37.p13 chr8: 134,514,865-134,520,436 ST3GAL1
    nsv6838518copy number variation1nstd229human GRCh38 chr8: 133,496,808-133,503,322 , GRCh37.p13 chr8: 134,509,051-134,515,565 ST3GAL1
    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