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 165

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141846copy number variation1nstd232human GRCh37.p13 chr19: 13,875,167-13,875,257 , GRCh38.p12 chr19: 13,764,353-13,764,443 MRI1
    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
    nsv7060894inversion1nstd229human GRCh38 chr19: 13,509,347-13,828,636 , GRCh37.p13 chr19: 13,620,161-13,939,450 C19orf53, LOC107985334, 6 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
    nsv7058723inversion1nstd229human GRCh38 chr19: 13,672,973-14,832,292 , GRCh37.p13 chr19: 13,783,787-14,943,104 SNRPGP15, NDUFB7, 53 more genes
    nsv7009682copy number variation1nstd229human GRCh38 chr19: 13,765,811-13,766,676 , GRCh37.p13 chr19: 13,876,625-13,877,490 MRI1
    nsv7005996copy number variation1nstd229human GRCh38 chr19: 13,725,201-13,895,200 , GRCh37.p13 chr19: 13,836,015-14,006,013 NANOS3, MIR23AHG, 12 more genes
    nsv7004965copy number variation1nstd229human GRCh38 chr19: 13,770,094-13,774,416 , GRCh37.p13 chr19: 13,880,908-13,885,230 MRI1, C19orf53
    nsv7003354copy number variation1nstd229human GRCh38 chr19: 13,761,025-13,764,401 , GRCh37.p13 chr19: 13,871,839-13,875,215 YJU2B, MRI1
    nsv7001637copy number variation1nstd229human GRCh38 chr19: 13,772,687-13,780,540 , GRCh37.p13 chr19: 13,883,501-13,891,354 C19orf53, MRI1
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6291633copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501 RN7SL619P, MIR6515, 67 more genes
    nsv6203333copy number variation1nstd214human GRCh38 chr19: 13,764,324-13,764,443 , GRCh37.p13 chr19: 13,875,138-13,875,257 MRI1
    nsv6201298copy number variation1nstd214human GRCh38 chr19: 13,764,324-13,764,395 , GRCh37.p13 chr19: 13,875,138-13,875,209 MRI1
    nsv6199643copy number variation1nstd214human GRCh38 chr19: 13,764,353-13,764,419 , GRCh37.p13 chr19: 13,875,167-13,875,233 MRI1
    nsv6191861copy number variation1nstd214human GRCh38 chr19: 13,764,725-13,764,780 , GRCh37.p13 chr19: 13,875,539-13,875,594 MRI1
    nsv6191428copy number variation1nstd214human GRCh38 chr19: 13,764,353-13,764,443 , GRCh37.p13 chr19: 13,875,167-13,875,257 MRI1
    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