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 175

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116797mobile element insertion1nstd186human GRCh37 chr17: 76,153,063-76,153,114 , GRCh38.p12 chr17: 78,156,982-78,157,033 EIF5AP2, C17orf99
    nsv5972596insertion1nstd209human GRCh38 chr17: 78,156,965-78,156,965 , GRCh37.p13 chr17: 76,153,046-76,153,046 C17orf99, EIF5AP2
    nsv5946583copy number variation1nstd209human GRCh38 chr17: 78,158,398-78,162,888 , GRCh37.p13 chr17: 76,154,479-76,158,969 EIF5AP2, C17orf99
    nsv5937287copy number variation1nstd209human GRCh38 chr17: 78,157,427-78,158,114 , GRCh37.p13 chr17: 76,153,508-76,154,195 EIF5AP2, C17orf99
    nsv5935743copy number variation1nstd209human GRCh38 chr17: 78,156,058-78,157,193 , GRCh37.p13 chr17: 76,152,139-76,153,274 C17orf99, EIF5AP2
    nsv5884277copy number variation1nstd209human GRCh38 chr17: 78,158,587-78,162,926 , GRCh37.p13 chr17: 76,154,668-76,159,007 EIF5AP2, C17orf99
    nsv5879087copy number variation1nstd209human GRCh38 chr17: 78,156,198-78,157,297 , GRCh37.p13 chr17: 76,152,279-76,153,378 EIF5AP2, C17orf99
    nsv5701681mobile element insertion2nstd211human GRCh38 chr17: 78,156,982-78,156,982 , GRCh37.p13 chr17: 76,153,063-76,153,063 C17orf99, EIF5AP2
    nsv5652261insertion1nstd207human GRCh38 chr17: 78,156,965-78,156,965 , GRCh37.p13 chr17: 76,153,046-76,153,046 EIF5AP2, C17orf99
    nsv5562557sequence alteration1nstd206human GRCh38 chr17: 78,156,150-78,158,462 , GRCh37.p13 chr17: 76,152,231-76,154,543 EIF5AP2, C17orf99
    nsv5524545copy number variation1nstd206human GRCh38 chr17: 78,157,432-78,158,115 , GRCh37.p13 chr17: 76,153,513-76,154,196 C17orf99, EIF5AP2
    nsv5415688mobile element insertion1nstd206human GRCh38 chr17: 78,156,982-78,157,033 , GRCh37.p13 chr17: 76,153,063-76,153,114 C17orf99, EIF5AP2
    nsv5349696translocation1nstd200human GRCh38 chr17: 78,158,435-78,158,435 , GRCh38 chr17: 78,162,889-78,162,889 , GRCh37.p13 chr17: 76,154,516-76,154,516 , GRCh37.p13 chr17: 76,158,970-76,158,970 EIF5AP2, C17orf99
    nsv5349695translocation1nstd200human GRCh38 chr17: 78,158,115-78,158,115 , GRCh38 chr17: 78,157,432-78,157,432 , GRCh37.p13 chr17: 76,154,196-76,154,196 , GRCh37.p13 chr17: 76,153,513-76,153,513 EIF5AP2, C17orf99
    nsv5336001translocation1nstd200human GRCh37 chr17: 76,154,196-76,154,196 , GRCh37 chr17: 76,153,513-76,153,513 , GRCh38.p12 chr17: 78,158,115-78,158,115 , GRCh38.p12 chr17: 78,157,432-78,157,432 EIF5AP2, C17orf99
    nsv5327810copy number variation1nstd204human GRCh37.p13 chr17: 76,154,506-76,158,979 , GRCh38.p13 chr17: 78,158,425-78,162,898 EIF5AP2, C17orf99
    nsv5322486copy number variation1nstd204human GRCh37.p13 chr17: 76,155,620-76,157,836 , GRCh38.p13 chr17: 78,159,539-78,161,755 EIF5AP2, C17orf99
    nsv5297999copy number variation1nstd204human GRCh38.p13 chr17: 78,158,401-78,163,000 , GRCh37.p13 chr17: 76,154,482-76,159,081 C17orf99, EIF5AP2
    nsv5295074copy number variation1nstd204human GRCh38.p13 chr17: 78,159,501-78,161,800 , GRCh37.p13 chr17: 76,155,582-76,157,881 EIF5AP2, C17orf99
    nsv5284853copy number variation1nstd204human GRCh38.p13 chr17: 78,158,574-78,162,738 , GRCh37.p13 chr17: 76,154,655-76,158,819 EIF5AP2, C17orf99
    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