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 9873

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3475160copy number variation10estd59human NCBI36 chr6: 139,270,029-139,318,357 , GRCh37.p13 chr6: 139,228,336-139,276,664 , GRCh38.p12 chr6: 138,907,199-138,955,527 REPS1
    esv3478069copy number variation50estd59human NCBI36 chr7: 128,944,399-128,991,457 , GRCh37.p13 chr7: 129,157,163-129,204,221 , GRCh38.p12 chr7: 129,517,322-129,564,380
    esv3320062copy number variation30estd59human NCBI36 chr10: 107,835,076-107,881,541 , GRCh37.p13 chr10: 107,845,086-107,891,551 , GRCh38.p12 chr10: 106,085,328-106,131,793 LOC105378469
    esv3453902copy number variation155estd59human NCBI36 chr20: 1,507,252-1,534,450 , GRCh37.p13 chr20: 1,559,252-1,586,450 , GRCh38.p12 chr20: 1,578,606-1,605,804 SIRPB1
    esv3453304copy number variation21estd59human NCBI36 chr1: 65,828,516-65,851,747 , GRCh37.p13 chr1: 66,055,928-66,079,159 , GRCh38.p12 chr1: 65,590,245-65,613,476 LEPR
    esv3419648copy number variation104estd59human NCBI36 chr11: 1,871,779-1,893,601 , GRCh37.p13 chr11: 1,915,203-1,937,025 , GRCh38.p12 chr11: 1,893,973-1,915,795 LINC01150
    esv3403910copy number variation109estd59human NCBI36 chr11: 1,871,732-1,893,611 , GRCh37.p13 chr11: 1,915,156-1,937,035 , GRCh38.p12 chr11: 1,893,926-1,915,805 LINC01150
    esv3464430copy number variation109estd59human NCBI36 chr4: 69,075,052-69,095,450 , GRCh37.p13 chr4: 69,392,457-69,412,855 , GRCh38.p12 chr4: 68,526,739-68,547,137 UGT2B17
    esv3475476copy number variation17estd59human NCBI36 chr7: 246,151-255,671 , GRCh37.p13 chr7: 151,068-160,588 , GRCh38.p12 chr7|NT_187558.1: 106,873-119,935 , GRCh38.p12 chr7: 151,068-160,588 , GRCh38.p12 chr7|NT_187653.1: 143,389-152,909 LINC03014
    esv3475478copy number variation28estd59human NCBI36 chr7: 246,136-255,715 , GRCh37.p13 chr7: 151,053-160,632 , GRCh38.p12 chr7: 151,053-160,632 , GRCh38.p12 chr7|NT_187558.1: 106,858-119,979 , GRCh38.p12 chr7|NT_187653.1: 143,374-152,953 LINC03014
    esv3475477copy number variation15estd59human NCBI36 chr7: 246,081-255,743 , GRCh37.p13 chr7: 150,998-160,660 , GRCh38.p12 chr7: 150,998-160,660 , GRCh38.p12 chr7|NT_187653.1: 143,319-152,981 , GRCh38.p12 chr7|NT_187558.1: 106,803-120,007 LINC03014
    esv3475474copy number variation16estd59human NCBI36 chr7: 246,182-255,671 , GRCh37.p13 chr7: 151,099-160,588 , GRCh38.p12 chr7|NT_187558.1: 106,904-119,935 , GRCh38.p12 chr7: 151,099-160,588 , GRCh38.p12 chr7|NT_187653.1: 143,420-152,909 LINC03014
    esv3315589copy number variation104estd59human NCBI36 chr17: 31,621,252-31,637,950 , GRCh37.p13 chr17: 34,597,139-34,613,837 , GRCh38.p12 chr17|NT_187661.1: 223,874-240,572 CCL3P1
    esv3484234copy number variation133estd59human NCBI36 chrX: 55,189,407-55,202,316 , GRCh37.p13 chrX: 55,172,682-55,185,591 , GRCh38.p12 chrX: 55,146,249-55,159,158 VCF2
    esv3480533copy number variation1estd59human NCBI36 chr8: 86,465,526-86,478,365 , GRCh37.p13 chr8: 86,278,274-86,291,113 , GRCh38.p12 chr8: 85,366,045-85,378,884 CA1
    esv3483204copy number variation58estd59human NCBI36 chr9: 112,064,315-112,076,985 , GRCh37.p13 chr9: 113,024,494-113,037,164 , GRCh38.p12 chr9: 110,262,214-110,274,884 LOC107987114
    esv3483205copy number variation31estd59human NCBI36 chr9: 112,064,258-112,077,009 , GRCh37.p13 chr9: 113,024,437-113,037,188 , GRCh38.p12 chr9: 110,262,157-110,274,908 LOC107987114
    esv3455536copy number variation16estd59human NCBI36 chr21: 10,118,517-10,130,466 , GRCh37.p13 chr21: 11,096,646-11,108,595 , GRCh38.p12 chr21: 10,403,833-10,415,782 BAGE2
    esv3477382copy number variation18estd59human NCBI36 chr7: 90,868,930-90,880,590 , GRCh37.p13 chr7: 91,030,994-91,042,654 , GRCh38.p12 chr7: 91,401,679-91,413,339 LINC02932
    esv3464428copy number variation112estd59human NCBI36 chr4: 69,063,352-69,078,450 , GRCh37.p13 chr4: 69,380,757-69,395,855 , GRCh38.p12 chr4: 68,515,039-68,530,137 UGT2B29P
    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