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 86

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3906080copy number variation1nstd102humanBenign GRCh37 chr16: 89,712,889-89,714,818 , GRCh38.p12 chr16: 89,646,481-89,648,410 CHMP1A
    nsv6137743copy number variation1nstd102humanBenign GRCh37 chr16: 89,715,541-89,715,605 , GRCh38 chr16: 89,649,133-89,649,197 CHMP1A
    nsv6310030copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,712,474-89,720,351 , GRCh38.p12 chr16: 89,646,066-89,653,943 CHMP1A
    nsv3922398copy number variation1nstd102humanLikely benign GRCh37 chr16: 89,653,087-89,714,891 , NCBI36 chr16: 88,180,588-88,242,392 , GRCh38 chr16: 89,586,679-89,648,483 CHMP1A, CPNE7, 1 more genes
    nsv4457573copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,666,802-89,760,599 , GRCh38.p12 chr16: 89,600,394-89,694,191 CHMP1A, DPEP1, 3 more genes
    nsv3907592copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,653,135-89,737,571 , GRCh38.p12 chr16: 89,586,727-89,671,163 CHMP1A, DPEP1, 2 more genes
    nsv7095117copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,712,474-89,866,066 , GRCh38.p12 chr16: 89,646,066-89,799,658 CHMP1A, FANCA, 7 more genes
    nsv6112808copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,620,873-89,881,041 , GRCh38.p12 chr16: 89,554,465-89,814,633 CHMP1A, CDK10, 12 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CHMP1A, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 CHMP1A, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 CHMP1A, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 CHMP1A, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 CHMP1A, 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 CHMP1A, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 CHMP1A, 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 CHMP1A, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 CHMP1A, 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 CHMP1A, 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 CHMP1A, 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 CHMP1A, MC1R, 528 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