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 21

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2763987copy number variation255estd203human NCBI36 chr6: 79,018,663-79,098,528 , GRCh37.p13 chr6: 78,961,944-79,041,809 , GRCh38.p12 chr6: 78,252,227-78,332,092 LOC105377865
    esv2762298copy number variation79estd203human NCBI36 chr1: 111,171,895-111,193,590 , GRCh37.p13 chr1: 111,370,372-111,392,067 , GRCh38.p12 chr1: 110,827,750-110,849,445 NRBF2P3
    esv2760688copy number variation119estd203human NCBI36 chr12: 726,126-746,507 , GRCh37.p13 chr12: 855,865-876,246 , GRCh38.p12 chr12: 746,699-767,080 WNK1
    esv2761844copy number variation1estd203human NCBI36 chr14: 73,361,692-73,366,404 , GRCh37.p13 chr14: 74,291,939-74,296,651 , GRCh38.p12 chr14: 73,825,236-73,829,948 LINC02274
    esv2763858copy number variation3estd203human NCBI36 chr1: 30,258,097-30,261,148 , GRCh37.p13 chr1: 30,485,510-30,488,561 , GRCh38.p12 chr1: 30,012,663-30,015,714 LINC01648
    esv2763839copy number variation49estd203human NCBI36 chr4: 173,224,402-173,233,468 , GRCh37.p13 chr4: 172,987,827-172,996,893 , GRCh38.p12 chr4: 172,066,676-172,075,742 GALNTL6
    esv2762743copy number variation368estd203human NCBI36 chr1: 72,522,436-72,595,424 , GRCh37.p13 chr1: 72,749,848-72,822,836 , GRCh38.p12 chr1: 72,284,165-72,357,153 , GRCh38.p12 chr1|NW_018654707.1: 1-78,378 RPL31P12, LOC105378797
    esv2761559copy number variation1estd203human GRCh38.p12 chr9: 130,228,134-130,260,065 , NCBI36 chr9: 132,030,234-132,062,165 , GRCh37.p13 chr9: 132,990,413-133,022,344 , GRCh37.p13 chr9|NW_004070869.1: 97,564-129,495 NCS1, MIR12126
    esv2762965copy number variation224estd203human NCBI36 chr1: 150,793,267-150,853,218 , GRCh37.p13 chr1: 152,526,643-152,586,594 , GRCh38.p12 chr1: 152,554,167-152,614,118 LCE3D, LCE3B, 2 more genes
    esv2764006copy number variation137estd203human NCBI36 chr7: 141,693,581-141,722,145 , GRCh37.p13 chr7|NW_003571040.1: 489,260-517,681 , GRCh38.p12 chr7|NT_187562.1: 309,189-330,225 TRB, TRBV6-2, 2 more genes
    esv2762632copy number variation122estd203human NCBI36 chr1: 25,455,216-25,589,952 , GRCh38.p12 chr1: 25,256,138-25,390,874 , GRCh37.p13 chr1: 25,582,629-25,717,365 RHCE, RHD, 4 more genes
    esv2761121copy number variation128estd203human NCBI36 chr13: 56,610,801-56,701,431 , GRCh38.p12 chr13: 57,138,666-57,229,296 , GRCh37.p13 chr13: 57,712,800-57,803,430 PRR20A, PRR20B, 6 more genes
    esv2761755copy number variation405estd203human NCBI36 chr15: 18,276,341-21,038,987 , GRCh37.p13 chr15: 20,016,328-23,487,546 , GRCh38.p12 chr15: 19,811,075-22,308,242 OR11K1P, LOC283804, 99 more genes
    esv2764166copy number variation266estd203human NCBI36 chr9: 43,255,666-44,936,428 , GRCh37.p13 chr9: 43,315,670-44,996,432 , GRCh38.p12 chr9: 41,912,139-42,974,549 SPATA31A6, ADGRF5P2, 30 more genes
    esv2761366copy number variation344estd203human NCBI36 chr14: 105,550,720-106,014,879 , GRCh37.p13 chr14: 106,479,675-106,943,834 , GRCh38.p12 chr14: 106,013,492-106,487,827 , GRCh38.p12 chr14|NT_187600.1: 475,711-1,214,078 IGH, IGHVIII-67-4, 116 more genes
    esv2764095copy number variation266estd203human NCBI36 chr8: 11,914,604-12,622,461 , GRCh37.p13 chr8: 11,877,195-12,578,090 , GRCh38.p12 chr8: 12,019,686-12,720,581 OR7E15P, FAM86B1, 38 more genes
    esv2762610copy number variation271estd203human NCBI36 chr17: 18,229,719-18,450,883 , GRCh37.p13 chr17: 18,288,994-18,510,158 , GRCh38.p12 chr17: 18,385,680-18,606,845 , GRCh38.p12 chr17|NW_017363819.1: 155,659-276,292 SRP68P2, CCDC144BP, 16 more genes
    esv2760075copy number variation2estd203human NCBI36 chr1: 194,095,134-194,141,530 , GRCh37.p13 chr1: 195,828,511-195,874,907 , GRCh38.p12 chr1: 195,859,381-195,905,777 0
    esv2763895copy number variation60estd203human NCBI36 chr5: 46,306,765-46,313,969 , GRCh37.p13 chr5: 46,271,008-46,278,212 , GRCh38.p12 chr5: 46,270,906-46,278,110 0
    esv2763628copy number variation41estd203human NCBI36 chr2: 106,246,527-106,251,789 , GRCh37.p13 chr2: 106,880,095-106,885,357 , GRCh38.p12 chr2: 106,263,639-106,268,901 0
    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