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 232

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5978481inversion1nstd209human GRCh38 chr12: 4,823,260-4,833,429 , GRCh37.p13 chr12: 4,932,426-4,942,595 KCNA6
    nsv5921920copy number variation1nstd209human GRCh38 chr12: 3,058,695-6,171,259 , GRCh37.p13 chr12: 3,167,861-6,280,425 , LOC105369623, 54 more genes
    nsv5704771mobile element insertion1nstd211human GRCh38 chr12: 4,849,516-4,849,516 , GRCh37.p13 chr12: 4,958,682-4,958,682 KCNA6
    nsv5585072copy number variation1nstd207human GRCh38 chr12: 4,828,051-4,828,127 , GRCh37.p13 chr12: 4,937,217-4,937,293 KCNA6
    nsv5564026inversion1nstd206human GRCh38 chr12: 4,823,225-4,833,465 , GRCh37.p13 chr12: 4,932,391-4,942,631 KCNA6
    nsv5381764copy number variation1nstd102humanPathogenic GRCh37 chr12: 3,619,010-5,221,363 , GRCh38.p12 chr12: 3,509,844-5,112,197 OTUD4P1, LOC105369612, 30 more genes
    nsv5380741copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,479,509-6,235,003 , GRCh38.p12 chr12: 4,370,343-6,125,837 ANO2, LOC105369617, 25 more genes
    nsv5348530translocation1nstd200human GRCh38 chr12: 4,843,841-4,843,841 , GRCh38 chr12: 4,843,910-4,843,910 , GRCh37.p13 chr12: 4,953,007-4,953,007 , GRCh37.p13 chr12: 4,953,076-4,953,076 KCNA6
    nsv5348528translocation1nstd200human GRCh38 chr12: 4,832,808-4,832,808 , GRCh38 chr12: 4,832,541-4,832,541 , GRCh37.p13 chr12: 4,941,974-4,941,974 , GRCh37.p13 chr12: 4,941,707-4,941,707 KCNA6
    nsv5348527translocation1nstd200human GRCh38 chr12: 4,820,363-4,820,363 , GRCh38 chr12: 4,846,373-4,846,373 , GRCh37.p13 chr12: 4,955,539-4,955,539 , GRCh37.p13 chr12: 4,929,529-4,929,529 KCNA6
    nsv5332215translocation1nstd200human GRCh37 chr12: 4,941,974-4,941,974 , GRCh37 chr12: 4,941,707-4,941,707 , GRCh38.p12 chr12: 4,832,541-4,832,541 , GRCh38.p12 chr12: 4,832,808-4,832,808 KCNA6
    nsv5315643copy number variation1nstd204human GRCh38.p13 chr12: 4,816,024-4,816,552 , GRCh37.p13 chr12: 4,925,190-4,925,718 KCNA6
    nsv5039014inversion1nstd200human GRCh38 chr12: 4,823,262-4,833,427 , GRCh37.p13 chr12: 4,932,428-4,942,593 KCNA6
    nsv4974253copy number variation1nstd200human GRCh38 chr12: 4,816,049-4,816,523 , GRCh37.p13 chr12: 4,925,215-4,925,689 KCNA6
    nsv4971941copy number variation1nstd200human GRCh38 chr12: 4,807,536-4,808,804 , GRCh37.p13 chr12: 4,916,702-4,917,970 , KCNA6
    nsv4872686inversion1nstd200human GRCh37 chr12: 4,932,428-4,942,595 , GRCh38.p12 chr12: 4,823,262-4,833,429 KCNA6
    nsv4847224copy number variation1nstd200human GRCh37 chr12: 4,916,702-4,917,970 , GRCh38.p12 chr12: 4,807,536-4,808,804 , KCNA6
    nsv4829948copy number variation1nstd200human GRCh37 chr12: 4,929,529-4,955,539 , GRCh38.p12 chr12: 4,820,363-4,846,373 KCNA6
    nsv4679795copy number variation1nstd189human GRCh37.p13 chr12: 4,504,235-4,966,214 , GRCh38.p12 chr12: 4,395,069-4,857,048 , FGF6, 10 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