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 1105

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130607mobile element insertion1nstd186human GRCh37 chr19: 39,256,101-39,256,145 , GRCh38.p12 chr19: 38,765,461-38,765,505 , GRCh38.p12 chr19|NW_014040929.1: 175,077-175,121 0
    nsv6130540insertion1nstd186human GRCh37 chr19: 39,227,244-39,227,272 , GRCh38.p12 chr19|NW_014040929.1: 146,207-146,235 , GRCh38.p12 chr19: 38,736,604-38,736,632 CAPN12
    nsv5391158copy number variation1nstd186human GRCh37 chr19: 39,234,138-39,234,348 , GRCh38.p12 chr19: 38,743,498-38,743,708 , GRCh38.p12 chr19|NW_014040929.1: 153,102-153,312 CAPN12
    nsv5390056copy number variation3nstd186human GRCh37 chr19: 39,240,835-39,240,960 , GRCh38.p12 chr19: 38,750,195-38,750,320 , GRCh38.p12 chr19|NW_014040929.1: 159,799-159,924 0
    nsv5340643translocation1nstd200human GRCh37 chr5: 107,979,678-107,979,678 , GRCh37 chr19: 39,287,137-39,287,137 , GRCh38.p12 chr5: 108,643,977-108,643,977 , GRCh38.p12 chr19: 38,796,497-38,796,497 , GRCh38.p12 chr19|NW_014040929.1: 206,179-206,179 RNU6-140P
    nsv5340224translocation1nstd200human GRCh37 chr19: 39,456,667-39,456,667 , GRCh37 chr19: 39,450,554-39,450,554 , GRCh38.p12 chr19|NW_014040929.1: 369,586-369,586 , GRCh38.p12 chr19: 38,959,914-38,959,914 , GRCh38.p12 chr19|NW_014040929.1: 375,699-375,699 , GRCh38.p12 chr19: 38,966,027-38,966,027 FBXO17
    nsv5339713translocation1nstd200human GRCh37 chr19: 39,456,357-39,456,357 , GRCh37 chr19: 39,457,871-39,457,871 , GRCh38.p12 chr19: 38,967,231-38,967,231 , GRCh38.p12 chr19|NW_014040929.1: 376,903-376,903 , GRCh38.p12 chr19|NW_014040929.1: 375,389-375,389 , GRCh38.p12 chr19: 38,965,717-38,965,717 FBXO17
    nsv5336198translocation1nstd200human GRCh37 chr19: 39,183,882-39,183,882 , GRCh37 chr19: 39,039,116-39,039,116 , GRCh38.p12 chr19: 38,548,476-38,548,476 , GRCh38.p12 chr19|NW_014040929.1: 102,878-102,878 , GRCh38.p12 chr19: 38,693,242-38,693,242 ACTN4, RYR1
    nsv5336130translocation1nstd200human GRCh37 chr2: 33,862,999-33,862,999 , GRCh37 chr19: 39,347,923-39,347,923 , GRCh38.p12 chr2: 33,637,932-33,637,932 , GRCh38.p12 chr19|NW_014040929.1: 266,955-266,955 , GRCh38.p12 chr19: 38,857,283-38,857,283 LOC105374455, HNRNPA1P61
    nsv5332424translocation1nstd200human GRCh37 chr19: 39,283,456-39,283,456 , GRCh37 chr19: 39,260,450-39,260,450 , GRCh38.p12 chr19|NW_014040929.1: 202,498-202,498 , GRCh38.p12 chr19: 38,769,810-38,769,810 , GRCh38.p12 chr19: 38,792,816-38,792,816 , GRCh38.p12 chr19|NW_014040929.1: 179,450-179,450 LGALS7
    nsv5331536translocation1nstd200human GRCh37 chr19: 39,348,289-39,348,289 , GRCh37 chr9: 24,093,114-24,093,114 , GRCh38.p12 chr9: 24,093,116-24,093,116 , GRCh38.p12 chr19: 38,857,649-38,857,649 , GRCh38.p12 chr19|NW_014040929.1: 267,321-267,321 0
    nsv4868314copy number variation1nstd200human GRCh37 chr19: 39,475,772-39,476,629 , GRCh38.p12 chr19: 38,985,132-38,985,989 , GRCh38.p12 chr19|NW_014040929.1: 394,804-395,661 0
    nsv4868313copy number variation1nstd200human GRCh37 chr19: 39,474,009-39,477,017 , GRCh38.p12 chr19|NW_014040929.1: 393,041-396,049 , GRCh38.p12 chr19: 38,983,369-38,986,377 0
    nsv4868312copy number variation1nstd200human GRCh37 chr19: 39,470,692-39,471,839 , GRCh38.p12 chr19: 38,980,052-38,981,199 , GRCh38.p12 chr19|NW_014040929.1: 389,724-390,871 0
    nsv4868311copy number variation1nstd200human GRCh37 chr19: 39,464,650-39,464,701 , GRCh38.p12 chr19: 38,974,010-38,974,061 , GRCh38.p12 chr19|NW_014040929.1: 383,682-383,733 FBXO17
    nsv4868310copy number variation1nstd200human GRCh37 chr19: 39,381,201-39,381,559 , GRCh38.p12 chr19: 38,890,561-38,890,919 , GRCh38.p12 chr19|NW_014040929.1: 300,233-300,591 SIRT2
    nsv4868309copy number variation1nstd200human GRCh37 chr19: 39,375,617-39,376,476 , GRCh38.p12 chr19|NW_014040929.1: 294,649-295,508 , GRCh38.p12 chr19: 38,884,977-38,885,836 SIRT2
    nsv4868308copy number variation1nstd200human GRCh37 chr19: 39,375,283-39,377,736 , GRCh38.p12 chr19: 38,884,643-38,887,096 , GRCh38.p12 chr19|NW_014040929.1: 294,315-296,768 SIRT2
    nsv4868307copy number variation1nstd200human GRCh37 chr19: 39,375,214-39,376,371 , GRCh38.p12 chr19: 38,884,574-38,885,731 , GRCh38.p12 chr19|NW_014040929.1: 294,246-295,403 SIRT2
    nsv4868306copy number variation1nstd200human GRCh37 chr19: 39,341,258-39,341,427 , GRCh38.p12 chr19|NW_014040929.1: 260,290-260,459 , GRCh38.p12 chr19: 38,850,618-38,850,787 HNRNPL
    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