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 113

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4759749inversion1nstd199human GRCh37 chr16: 70,151,143-74,397,976 , GRCh38.p12 chr16: 70,117,240-74,364,078 , AARS1, 85 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4683237copy number variation1nstd102humanPathogenic GRCh37 chr16: 71,603,737-71,610,338 , GRCh38.p12 chr16: 71,569,834-71,576,435 TAT-AS1, TAT
    nsv4550921insertion1nstd166human GRCh37.p13 chr16: 71,606,412-71,606,412 , GRCh38.p12 chr16: 71,572,509-71,572,509 TAT, TAT-AS1
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4377066copy number variation1nstd173human GRCh37 chr16: 70,197,501-72,654,326 , GRCh38.p12 chr16: 70,163,598-72,620,427 , LOC102725168, 67 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4321328inversion1nstd166human GRCh37.p13 chr16: 67,701,568-75,754,137 , GRCh38.p12 chr16: 67,667,665-75,720,239 , CDH3, 203 more genes
    nsv3969586inversion1nstd168human GRCh38 chr16: 70,195,952-74,390,641 , GRCh37.p13 chr16: 70,229,855-74,424,539 , AARS1, 82 more genes
    nsv3922890copy number variation1nstd102humanPathogenic GRCh37 chr16: 70,783,301-90,163,403 , GRCh38 chr16: 70,749,398-90,096,995 , NCBI36 chr16: 69,340,802-88,690,904 GCSH, LOC390739, 362 more genes
    nsv3922616copy number variation1nstd102humanPathogenic GRCh38 chr16: 70,514,631-90,081,985 , NCBI36 chr16: 69,106,035-88,675,894 , GRCh37 chr16: 70,548,534-90,148,393 FOXF1, RNA5SP431, 367 more genes
    nsv3922126copy number variation1nstd102humanPathogenic NCBI36 chr16: 67,644,861-81,865,787 , GRCh38 chr16: 69,053,457-83,274,681 , GRCh37 chr16: 69,087,360-83,308,286 LOC105371357, EXOSC6, 232 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3921095copy number variation1nstd102humanPathogenic NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726 NECAB2, CENPN-AS1, 219 more genes
    nsv3920399copy number variation1nstd102humanPathogenic NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795 LOC654780, LSM3P5, 385 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