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 131

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095645copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315 HAUS8, MIR1470, 95 more genes
    nsv7075473inversion1nstd229human GRCh38 chr19: 12,694,752-17,614,167 , GRCh37.p13 chr19: 12,805,566-17,724,976 SYDE1, LOC107985287, 207 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7063135inversion1nstd229human GRCh38 chr19: 12,625,698-17,530,884 , GRCh37.p13 chr19: 12,736,512-17,641,693 SYCE2, OR1AB1P, 212 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7004911copy number variation1nstd229human GRCh38 chr19: 16,817,573-17,564,195 , GRCh37.p13 chr19: 16,928,384-17,675,004 BISPR, NWD1, 32 more genes
    nsv7001566copy number variation1nstd229human GRCh38 chr19: 16,881,794-16,888,516 , GRCh37.p13 chr19: 16,992,605-16,999,327 F2RL3
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6525646copy number variation1nstd223human GRCh38 chr19: 16,886,123-16,942,236 , GRCh37.p13 chr19: 16,996,934-17,053,046 RN7SL835P, F2RL3, 2 more genes
    nsv6524788copy number variation1nstd223human GRCh38 chr19: 16,887,138-16,888,505 , GRCh37.p13 chr19: 16,997,949-16,999,316 F2RL3
    nsv6133691copy number variation1nstd213human GRCh37 chr19: 15,360,000-18,450,001 , GRCh38.p12 chr19: 15,249,189-18,339,191 BST2, NR2F6, 123 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5518048copy number variation1nstd206human GRCh38 chr19: 16,886,978-16,887,297 , GRCh37.p13 chr19: 16,997,789-16,998,108 F2RL3
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014609copy number variation1nstd200human GRCh38 chr19: 16,886,050-16,942,375 , GRCh37.p13 chr19: 16,996,861-17,053,185 CPAMD8, F2RL3, 2 more genes
    nsv4860544copy number variation1nstd200human GRCh37 chr19: 17,002,212-17,002,526 , GRCh38.p12 chr19: 16,891,401-16,891,715 CPAMD8, F2RL3
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4457871copy number variation1nstd102humanUncertain significance GRCh37 chr19: 16,875,725-17,477,318 , GRCh38.p12 chr19: 16,764,914-17,366,509 HAUS8, MYO9B, 19 more genes
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 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