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 195

    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
    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
    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
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5884215copy number variation2nstd209human GRCh38 chr21: 13,096,557-13,106,633 , GRCh37.p13 chr21: 14,468,878-14,478,954 ZNF355P, ANKRD30BP2
    nsv5586318copy number variation1nstd207human GRCh38 chr21: 13,097,589-13,097,756 , GRCh37.p13 chr21: 14,469,910-14,470,077 ZNF355P, ANKRD30BP2
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5523615copy number variation1nstd206human GRCh38 chr21: 13,094,289-13,094,380 , GRCh37.p13 chr21: 14,466,610-14,466,701 ZNF355P, ANKRD30BP2
    nsv5300285copy number variation1nstd204human GRCh38.p13 chr21: 13,070,138-13,098,909 , GRCh37.p13 chr21: 14,442,459-14,471,230 VN1R109P, ZNF355P, 1 more genes
    nsv5294664copy number variation1nstd204human GRCh38.p13 chr21: 13,091,001-13,120,100 , GRCh37.p13 chr21: 14,463,322-14,492,421 ANKRD30BP2, ZNF355P, 1 more genes
    nsv5292901copy number variation1nstd204human GRCh38.p13 chr21: 13,091,001-13,094,600 , GRCh37.p13 chr21: 14,463,322-14,466,921 ANKRD30BP2, ZNF355P, 1 more genes
    nsv5282452copy number variation1nstd204human GRCh38.p13 chr21: 13,094,601-13,097,800 , GRCh37.p13 chr21: 14,466,922-14,470,121 ANKRD30BP2, ZNF355P
    nsv5282366copy number variation1nstd204human GRCh38.p13 chr21: 13,037,701-13,120,000 , GRCh37.p13 chr21: 14,410,022-14,492,321 RNU6-614P, ANKRD30BP2, 2 more genes
    nsv5280553copy number variation1nstd204human GRCh38.p13 chr21: 13,037,601-13,109,200 , GRCh37.p13 chr21: 14,409,922-14,481,521 ANKRD30BP2, RNU6-614P, 2 more genes
    nsv4680842copy number variation1nstd189human GRCh37.p13 chr21: 14,446,713-15,137,079 , GRCh38.p12 chr21: 13,074,392-13,764,758 VN1R8P, OR4K12P, 20 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