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
    esv3817884copy number variation1789estd214human GRCh37 chrX: 131,089,382-131,089,611 , GRCh38.p12 chrX: 131,955,354-131,955,583 0
    esv3817679copy number variation1848estd214human GRCh37 chrX: 147,509,695-147,511,237 , GRCh38.p12 chrX: 148,428,176-148,429,718 0
    esv3817610mobile element insertion1552estd214human GRCh37 chrX: 126,290,693-126,290,693 , GRCh38.p12 chrX: 127,156,710-127,156,710 0
    esv3817420copy number variation904estd214human GRCh37 chrX: 115,137,622-115,153,304 , GRCh38.p12 chr: NaN-NaN 0
    esv3817830copy number variation962estd214human GRCh37 chrX: 33,712,708-33,713,545 , GRCh38.p12 chrX: 33,694,591-33,695,428 0
    esv3816956copy number variation1245estd214human GRCh37 chrX: 97,167,898-97,168,316 , GRCh38.p12 chrX: 97,912,900-97,913,318 0
    esv3817449copy number variation31estd214human GRCh37 chrX: 89,893,285-89,911,699 , GRCh38.p12 chrX: 90,638,286-90,656,700 0
    esv3817250copy number variation1086estd214human GRCh37 chrX: 80,572,069-80,573,144 , GRCh38.p12 chrX: 81,316,570-81,317,645 0
    esv3817540delins614estd214human GRCh37 chrX: 4,379,955-4,379,955 , GRCh38.p12 chrX: 4,461,914-4,461,914 0
    esv3817429copy number variation449estd214human GRCh37 chrX: 45,016,239-45,017,623 , GRCh38.p12 chrX: 45,156,994-45,158,378 DIPK2B
    esv3817800copy number variation625estd214human GRCh37 chrX: 70,137,259-70,139,986 , GRCh38.p12 chrX: 70,917,409-70,920,136 0
    esv3817036delins351estd214human GRCh37 chrX: 78,724,856-78,724,856 , GRCh38.p12 chrX: 79,469,359-79,469,359 0
    esv3817803delins239estd214human GRCh37 chrX: 40,822,590-40,822,590 , GRCh38.p12 chrX: 40,963,337-40,963,337 0
    esv3817520copy number variation733estd214human GRCh37 chrX: 91,678,126-91,680,088 , GRCh38.p12 chrX: 92,423,127-92,425,089 PCDH11X
    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
    esv3817548delins741estd214human GRCh37 chrX: 88,739,727-88,739,727 , GRCh38.p12 chrX: 89,484,728-89,484,728 0
    esv3817894delins1812estd214human GRCh37 chrX: 146,888,810-146,888,810 , GRCh38.p12 chrX: 147,807,292-147,807,292 0
    esv3817177copy number variation2006estd214human GRCh37 chrX: 90,283,367-90,284,081 , GRCh38.p12 chrX: 91,028,368-91,029,082 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