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 425

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6626815copy number variation1nstd224human GRCh37 chr21: 14,359,894-14,824,503 , GRCh38.p12 chr21: 12,987,573-13,452,182 ANKRD30BP2, GTF2IP2, 6 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6554425copy number variation1nstd223human GRCh38 chr21: 13,040,001-13,047,900 , GRCh37.p13 chr21: 14,412,322-14,420,221 RNU6-614P, ANKRD30BP2
    nsv6548211copy number variation1nstd223human GRCh38 chr21: 13,052,401-13,370,500 , GRCh37.p13 chr21: 14,424,722-14,742,821 ANKRD30BP2, VN1R109P, 2 more genes
    nsv6545872copy number variation1nstd223human GRCh38 chr21: 13,045,301-13,087,100 , GRCh37.p13 chr21: 14,417,622-14,459,421 ANKRD30BP2, RNU6-614P
    nsv6543918copy number variation1nstd223human GRCh38 chr21: 13,045,301-13,191,400 , GRCh37.p13 chr21: 14,417,622-14,563,721 VN1R109P, ANKRD30BP2, 2 more genes
    nsv6542904copy number variation1nstd223human GRCh38 chr21: 13,091,001-13,120,000 , GRCh37.p13 chr21: 14,463,322-14,492,321 VN1R109P, ANKRD30BP2, 1 more genes
    nsv6536437copy number variation1nstd223human GRCh38 chr21: 13,047,401-13,188,300 , GRCh37.p13 chr21: 14,419,722-14,560,621 RNU6-614P, VN1R109P, 2 more genes
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
    nsv6289996copy number variation1nstd102humanPathogenic GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 KRTAP7-1, MAP3K7CL, 656 more genes
    nsv6288269insertion1nstd214human GRCh38 chr21: 13,049,792-13,049,792 , GRCh37.p13 chr21: 14,422,113-14,422,113 ANKRD30BP2
    nsv6287458insertion3nstd214human GRCh38 chr21: 13,049,750-13,049,750 , GRCh37.p13 chr21: 14,422,071-14,422,071 ANKRD30BP2
    nsv6286252insertion1nstd214human GRCh38 chr21: 13,049,778-13,049,778 , GRCh37.p13 chr21: 14,422,099-14,422,099 ANKRD30BP2
    nsv6251643mobile element insertion1nstd215human GRCh38 chr21: 13,068,783-13,068,783 , GRCh37.p13 chr21: 14,441,104-14,441,104 ANKRD30BP2
    nsv6212527copy number variation1nstd214human GRCh38 chr21: 13,117,742-13,117,822 , GRCh37.p13 chr21: 14,490,063-14,490,143 ANKRD30BP2
    nsv6146440copy number variation1nstd206human GRCh38 chr21: 13,041,808-13,047,808 , GRCh37.p13 chr21: 14,414,129-14,420,129 ANKRD30BP2, RNU6-614P
    nsv6146231copy number variation1nstd206human GRCh38 chr21: 13,087,467-13,087,543 , GRCh37.p13 chr21: 14,459,788-14,459,864 ANKRD30BP2
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6106552insertion1nstd212human GRCh38 chr21: 13,042,673-13,042,673 , GRCh37.p13 chr21: 14,414,994-14,414,994 ANKRD30BP2
    nsv6105397insertion1nstd212human GRCh38 chr21: 13,049,750-13,049,750 , GRCh37.p13 chr21: 14,422,071-14,422,071 ANKRD30BP2
    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