U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 51

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 ZNF821, NECAB2, 219 more genes
    nsv3917504copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,951,979-76,757,245 , NCBI36 chr16: 68,509,480-75,314,746 , GRCh38 chr16: 69,918,076-76,723,348 ZNF821, TRG-GCC3-1, 137 more genes
    nsv3916803copy number variation1nstd102humanPathogenic NCBI36 chr16: 68,126,727-74,517,697 , GRCh37.p13 chr16: 69,569,226-75,960,196 , GRCh38.p12 chr16: 69,535,323-75,926,298 ZNF821, AP1G1, 138 more genes
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 ZNF821, ZNF19, 128 more genes
    nsv3911569copy number variation1nstd102humanPathogenic GRCh38 chr16: 68,698,941-74,353,205 , NCBI36 chr16: 67,290,345-72,944,604 , GRCh37 chr16: 68,732,844-74,387,103 ZNF821, ATP5F1AP3, 121 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 ZNF821, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 ZNF821, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 ZNF821, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 ZNF821, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 ZNF821, FTLP14, 1868 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 ZNF821, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ZNF821, ATMIN, 826 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 ZNF821, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 ZNF821, LOC107984894, 613 more genes
    nsv3913913copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393 ZNF821, ATP5F1AP3, 534 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 ZNF821, LOC105376772, 527 more genes
    nsv3910304copy number variation1nstd102humanPathogenic NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403 ZNF821, MC1R, 528 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 ZNF821, LOC654780, 385 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 ZNF821, FOXF1, 367 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 ZNF821, GCSH, 362 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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