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 97

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891800copy number variation1nstd209human GRCh38 chr6: 33,337,248-33,349,967 , GRCh37.p13 chr6: 33,305,025-33,317,744 MYL12BP3
    nsv5378375translocation1nstd200human GRCh38 chr6: 33,339,738-33,339,738 , GRCh38 chr7: 81,419,138-81,419,138 , GRCh37.p13 chr6: 33,307,515-33,307,515 , GRCh37.p13 chr7: 81,048,454-81,048,454 MYL12BP3
    nsv5231786copy number variation1nstd204human GRCh38.p13 chr6: 33,016,601-33,499,100 , GRCh37.p13 chr6: 32,984,378-33,466,877 COL11A2, RXRB, 39 more genes
    nsv4828619copy number variation1nstd200human GRCh37 chr6: 33,305,025-33,317,746 , GRCh38.p12 chr6: 33,337,248-33,349,969 MYL12BP3
    nsv4778582mobile element deletion1nstd200human GRCh37 chr6: 33,305,444-33,305,767 , GRCh38.p12 chr6: 33,337,667-33,337,990 MYL12BP3
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4682849copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926 RPL35AP4, RGL2, 29 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4451881copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926 COL11A2, HSD17B8, 29 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3955504copy number variation1nstd168human GRCh38 chr6: 33,320,444-33,338,903 , GRCh37.p13 chr6: 33,288,221-33,306,680 MYL12BP3, DAXX, 1 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 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