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 5031

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5665124copy number variation1nstd207human GRCh38 chrX: 127,625,450-127,752,681 , GRCh37.p13 chrX: 126,759,431-126,886,662 LOC100420320
    nsv5588287copy number variation1nstd207human GRCh38 chr18: 15,162,839-15,208,410 , GRCh37.p13 chr18: 15,162,838-15,208,409 LOC112268217
    nsv5587456copy number variation1nstd207human GRCh38 chr11: 7,789,629-7,811,833 , GRCh37.p13 chr11: 7,811,176-7,833,380 OR5P2
    nsv5571222copy number variation1nstd207human GRCh38 chr1: 246,205,582-246,225,470 , GRCh37.p13 chr1: 246,368,884-246,388,772 SMYD3
    nsv5575875copy number variation1nstd207human GRCh38 chr2: 73,783,733-73,803,332 , GRCh37.p13 chr2: 74,010,860-74,030,459 C2orf78
    nsv5670832copy number variation1nstd207human GRCh38 chrX: 108,364,720-108,379,714 , GRCh37.p13 chrX: 107,607,950-107,622,944 COL4A6
    nsv5571979copy number variation1nstd207human GRCh38 chr2: 188,703,110-188,715,940 , GRCh37.p13 chr2: 189,567,837-189,580,667 LOC105373790
    nsv5596277copy number variation1nstd207human GRCh38 chr11: 46,466,355-46,477,951 , GRCh37.p13 chr11: 46,487,905-46,499,501 AMBRA1
    nsv5574589copy number variation1nstd207human GRCh38 chr8: 136,682,003-136,693,454 , GRCh37.p13 chr8: 137,694,246-137,705,697 LINC02055
    nsv5604168copy number variation1nstd207human GRCh38 chr9: 62,087,560-62,098,925 , GRCh37.p13 chr9: 45,223,712-45,235,077 LOC107987008
    nsv5574346copy number variation1nstd207human GRCh38 chr6: 122,538,342-122,547,637 , GRCh37.p13 chr6: 122,859,487-122,868,782 PKIB
    nsv5571383copy number variation1nstd207human GRCh38 chr6: 26,676,987-26,686,095 , GRCh37.p13 chr6|NW_004070866.1: 91,373-100,481 , GRCh37.p13 chr6: 26,677,215-26,686,323 LOC102724851
    nsv5601506copy number variation1nstd207human GRCh38 chr17: 80,018,213-80,027,041 , GRCh37.p13 chr17: 77,992,012-78,000,840 TBC1D16
    nsv5594055copy number variation1nstd207human GRCh38 chr10: 28,275,654-28,283,761 , GRCh37.p13 chr10: 28,564,583-28,572,690 MPP7
    nsv5569768copy number variation1nstd207human GRCh38 chr5: 19,956,495-19,964,577 , GRCh37.p13 chr5: 19,956,604-19,964,686 CDH18
    nsv5588602copy number variation1nstd207human GRCh38 chr20: 14,291,367-14,298,816 , GRCh37.p13 chr20: 14,272,013-14,279,462 MACROD2
    nsv5592711copy number variation1nstd207human GRCh38 chr11: 36,625,907-36,633,260 , GRCh37.p13 chr11: 36,647,457-36,654,810 IFTAP
    nsv5583155copy number variation1nstd207human GRCh38 chr8: 84,612,550-84,619,804 , GRCh37.p13 chr8: 85,524,785-85,532,039 RALYL
    nsv5603524copy number variation1nstd207human GRCh38 chr13: 48,204,516-48,211,648 , GRCh37.p13 chr13: 48,778,652-48,785,784 LOC105370198
    nsv5571144copy number variation1nstd207human GRCh38 chr3: 4,152,419-4,159,492 , GRCh37.p13 chr3: 4,194,103-4,201,176 SUMF1
    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