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 4270

    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
    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
    esv3817679copy number variation1848estd214human GRCh37 chrX: 147,509,695-147,511,237 , GRCh38.p12 chrX: 148,428,176-148,429,718 0
    esv3817413delins1094estd214human GRCh37 chrX: 319,122-319,122 , GRCh38.p12 chrX: 358,387-358,387 , GRCh38.p12 chrX|NT_187667.1: 30,880-30,880 , GRCh38.p12 chrX|NT_187634.1: 41,740-41,740 PPP2R3B
    esv3817154copy number variation887estd214human GRCh37 chrX: 32,886,342-32,886,931 , GRCh38.p12 chrX: 32,868,225-32,868,814 DMD
    esv3817694copy number variation502estd214human GRCh37 chrX: 24,184,245-24,185,065 , GRCh38.p12 chrX: 24,166,128-24,166,948 ZFX
    esv3817250copy number variation1086estd214human GRCh37 chrX: 80,572,069-80,573,144 , GRCh38.p12 chrX: 81,316,570-81,317,645 0
    esv3817710copy number variation1286estd214human GRCh37 chrX: 78,921,957-78,926,007 , GRCh38.p12 chrX: 79,666,460-79,670,510 0
    esv3817158copy number variation1708estd214human GRCh37 chrX: 69,302,587-69,303,799 , GRCh38.p12 chrX: 70,082,737-70,083,949 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
    esv3817183copy number variation1107estd214human GRCh37 chrX: 32,987,321-32,989,080 , GRCh38.p12 chrX: 32,969,204-32,970,963 DMD
    esv3817162delins857estd214human GRCh37 chrX: 57,724,536-57,724,536 , GRCh38.p12 chrX: 57,698,103-57,698,103 0
    esv3817838mobile element insertion1218estd214human GRCh37 chrX: 2,699,520-2,699,520 , GRCh38.p12 chrX: 2,781,479-2,781,479 XG
    esv3818037copy number variation706estd214human GRCh37 chrY: 6,543,373-6,559,148 , GRCh38.p12 chrY: 6,675,332-6,691,107 0
    esv3817177copy number variation2006estd214human GRCh37 chrX: 90,283,367-90,284,081 , GRCh38.p12 chrX: 91,028,368-91,029,082 0
    esv3817463mobile element insertion475estd214human GRCh37 chrX: 116,025,285-116,025,285 , GRCh38.p12 chrX: 116,891,317-116,891,317 0
    esv3817119copy number variation1054estd214human GRCh37 chrX: 144,887,117-144,887,540 , GRCh38.p12 chrX: 145,805,599-145,806,022 0
    esv3817350delins2157estd214human GRCh37 chrX: 19,485,813-19,485,813 , GRCh38.p12 chrX: 19,467,695-19,467,695 MAP3K15
    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