U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from BioSample

Items: 1 to 20 of 998

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3817218delins1586estd214human GRCh37 chrX: 1,018,298-1,018,298 , GRCh38.p12 chrX: 1,057,563-1,057,563 0
    esv3817754mobile element insertion601estd214human GRCh37 chrX: 14,152,015-14,152,015 , GRCh38.p12 chrX: 14,133,896-14,133,896 0
    esv3817884copy number variation1789estd214human GRCh37 chrX: 131,089,382-131,089,611 , GRCh38.p12 chrX: 131,955,354-131,955,583 0
    esv3817195copy number variation1683estd214human GRCh37 chrX: 910,112-910,847 , GRCh38.p12 chrX: 949,377-950,112 0
    esv3817633copy number variation942estd214human GRCh37 chrX: 153,733,758-153,734,289 , GRCh38.p12 chrX: 154,505,427-154,505,958 FAM3A
    esv3817420copy number variation904estd214human GRCh37 chrX: 115,137,622-115,153,304 , GRCh38.p12 chr: NaN-NaN 0
    esv3817665copy number variation259estd214human GRCh37 chrX: 1,437,891-1,438,937 , GRCh38.p12 chrX: 1,318,998-1,320,044 CSF2RA
    esv3817191copy number variation775estd214human GRCh37 chrX: 153,634,830-153,636,529 , GRCh38.p12 chrX: 154,406,489-154,408,193 DNASE1L1
    esv3817070copy number variation1108estd214human GRCh37 chrX: 22,377,617-22,378,107 , GRCh38.p12 chrX: 22,359,500-22,359,990 PTCHD1-AS
    esv3817466copy number variation745estd214human GRCh37 chrX: 105,938,828-105,939,512 , GRCh38.p12 chrX: 106,695,598-106,696,282 RNF128
    esv3817827mobile element insertion168estd214human GRCh37 chrX: 127,763,536-127,763,536 , GRCh38.p12 chrX: 128,629,558-128,629,558 LOC107985698
    esv3817661copy number variation1165estd214human GRCh37 chrX: 154,778,170-154,778,667 , GRCh38.p12 chrX: 155,548,509-155,549,006 TMLHE
    esv3816943mobile element insertion984estd214human GRCh37 chrX: 55,585,160-55,585,160 , GRCh38.p12 chrX: 55,558,727-55,558,727 0
    esv3817710copy number variation1286estd214human GRCh37 chrX: 78,921,957-78,926,007 , GRCh38.p12 chrX: 79,666,460-79,670,510 0
    esv3817540delins614estd214human GRCh37 chrX: 4,379,955-4,379,955 , GRCh38.p12 chrX: 4,461,914-4,461,914 0
    esv3817530copy number variation817estd214human GRCh37 chrX: 107,627,859-107,628,663 , GRCh38.p12 chrX: 108,384,629-108,385,433 COL4A6
    esv3817553copy number variation685estd214human GRCh37 chrX: 28,697,448-28,698,860 , GRCh38.p12 chrX: 28,679,331-28,680,743 IL1RAPL1
    esv3817473mobile element insertion90estd214human GRCh37 chrX: 143,420,722-143,420,722 , GRCh38.p12 chrX: 144,337,599-144,337,599 0
    esv3817458copy number variation1061estd214human GRCh37 chrX: 131,744,448-131,745,660 , GRCh38.p12 chrX: 132,610,420-132,611,632 0
    esv3817327copy number variation2251estd214human GRCh37 chrX: 144,422,074-144,424,508 , GRCh38.p12 chrX: 145,340,556-145,342,990 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