U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 569

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6621205copy number variation1nstd224human GRCh37 chr11: 7,817,666-7,847,348 , GRCh38.p12 chr11: 7,796,119-7,825,801 , GRCh38.p12 chr11|NT_187583.1: 16,987-46,669 , GRCh38.p12 chr11|NW_011332695.1: 16,987-56,791 OR5P2, OR5P3
    nsv6621023copy number variation2nstd224human GRCh37 chr11: 7,780,767-7,950,121 , GRCh38.p12 chr11: 7,759,220-7,928,574 , GRCh38.p12 chr11|NT_187583.1: 1-160,075 , GRCh38.p12 chr11|NW_011332695.1: 1-159,568 OR5E1P, OR5P1P, 7 more genes
    nsv6305490copy number variation1nstd186human GRCh37 chr11: 7,861,381-7,861,510 , GRCh38.p12 chr11: 7,839,834-7,839,963 , GRCh38.p12 chr11|NW_011332695.1: 70,828-70,957 , GRCh38.p12 chr11|NT_187583.1: 60,702-60,831 0
    nsv6292312mobile element insertion1nstd186human GRCh37 chr11: 7,874,735-7,874,786 , GRCh38.p12 chr11|NT_187583.1: 84,704-84,755 , GRCh38.p12 chr11: 7,853,188-7,853,239 , GRCh38.p12 chr11|NW_011332695.1: 84,182-84,233 LOC283299
    nsv5392335copy number variation1nstd186human GRCh37 chr11: 7,846,670-7,847,197 , GRCh38.p12 chr11|NT_187583.1: 45,991-46,518 , GRCh38.p12 chr11|NW_011332695.1: 56,113-56,640 , GRCh38.p12 chr11: 7,825,123-7,825,650 OR5P3
    nsv4848895copy number variation1nstd200human GRCh37 chr11: 7,972,637-7,975,895 , GRCh38.p12 chr11: 7,951,090-7,954,348 , GRCh38.p12 chr11|NT_187583.1: 182,591-185,849 , GRCh38.p12 chr11|NW_011332695.1: 182,084-185,342 0
    nsv4847588copy number variation1nstd200human GRCh37 chr11: 7,945,993-7,946,532 , GRCh38.p12 chr11|NT_187583.1: 155,947-156,486 , GRCh38.p12 chr11|NW_011332695.1: 155,440-155,979 , GRCh38.p12 chr11: 7,924,446-7,924,985 0
    nsv4846156copy number variation1nstd200human GRCh37 chr11: 7,846,668-7,847,200 , GRCh38.p12 chr11|NT_187583.1: 45,989-46,521 , GRCh38.p12 chr11: 7,825,121-7,825,653 , GRCh38.p12 chr11|NW_011332695.1: 56,111-56,643 OR5P3
    nsv4845412copy number variation1nstd200human GRCh37 chr11: 7,905,900-7,906,614 , GRCh38.p12 chr11|NT_187583.1: 115,854-116,568 , GRCh38.p12 chr11: 7,884,353-7,885,067 , GRCh38.p12 chr11|NW_011332695.1: 115,347-116,061 LOC283299
    nsv4843521copy number variation1nstd200human GRCh37 chr11: 7,939,466-7,949,849 , GRCh38.p12 chr11: 7,917,919-7,928,302 , GRCh38.p12 chr11|NT_187583.1: 149,420-159,803 , GRCh38.p12 chr11|NW_011332695.1: 148,913-159,296 OR10A6
    nsv4839968copy number variation1nstd200human GRCh37 chr11: 7,815,392-7,815,638 , GRCh38.p12 chr11|NT_187583.1: 14,713-14,959 , GRCh38.p12 chr11: 7,793,845-7,794,091 , GRCh38.p12 chr11|NW_011332695.1: 14,713-14,959 OR5P2
    nsv4839534copy number variation1nstd200human GRCh37 chr11: 7,811,176-7,833,378 , GRCh38.p12 chr11: 7,789,629-7,811,831 , GRCh38.p12 chr11|NW_011332695.1: 10,497-32,701 , GRCh38.p12 chr11|NT_187583.1: 10,497-32,699 OR5P2
    nsv4837690copy number variation1nstd200human GRCh37 chr11: 7,846,664-7,847,578 , GRCh38.p12 chr11|NW_011332695.1: 56,107-57,021 , GRCh38.p12 chr11|NT_187583.1: 45,985-46,899 , GRCh38.p12 chr11: 7,825,117-7,826,031 OR5P3
    nsv4836903copy number variation1nstd200human GRCh37 chr11: 7,856,790-7,864,813 , GRCh38.p12 chr11|NW_011332695.1: 66,237-74,260 , GRCh38.p12 chr11|NT_187583.1: 56,111-64,139 , GRCh38.p12 chr11: 7,835,243-7,843,266 0
    nsv4834598copy number variation1nstd200human GRCh37 chr11: 7,963,911-7,973,490 , GRCh38.p12 chr11: 7,942,364-7,951,943 , GRCh38.p12 chr11|NW_011332695.1: 173,358-182,937 , GRCh38.p12 chr11|NT_187583.1: 173,865-183,444 0
    nsv4833972copy number variation1nstd200human GRCh37 chr11: 7,839,805-7,840,531 , GRCh38.p12 chr11|NT_187583.1: 39,126-39,852 , GRCh38.p12 chr11: 7,818,258-7,818,984 , GRCh38.p12 chr11|NW_011332695.1: 49,249-49,975 0
    nsv4832904copy number variation1nstd200human GRCh37 chr11: 7,947,894-7,951,289 , GRCh38.p12 chr11|NT_187583.1: 157,848-161,243 , GRCh38.p12 chr11: 7,926,347-7,929,742 , GRCh38.p12 chr11|NW_011332695.1: 157,341-160,736 OR10A6
    nsv4829770copy number variation1nstd200human GRCh37 chr11: 7,987,126-7,993,012 , GRCh38.p12 chr11|NW_011332695.1: 196,573-202,459 , GRCh38.p12 chr11: 7,965,579-7,971,465 , GRCh38.p12 chr11|NT_187583.1: 197,080-202,966 NLRP10
    nsv4768981insertion1nstd186human GRCh37 chr11: 7,866,094-7,866,094 , GRCh38.p12 chr11: 7,844,547-7,844,547 , GRCh38.p12 chr11|NT_187583.1: 65,421-65,421 , GRCh38.p12 chr11|NW_011332695.1: 75,541-75,541 0
    nsv4751153insertion1nstd199human GRCh37 chr11: 7,866,096-7,866,096 , GRCh38.p12 chr11: 7,844,549-7,844,549 , GRCh38.p12 chr11|NT_187583.1: 65,423-65,423 , GRCh38.p12 chr11|NW_011332695.1: 75,543-75,543 0
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    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