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 2662

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3817210copy number variation589estd214human GRCh37 chrX: 61,950,926-61,955,115 , GRCh38.p12 chrX: 62,731,456-62,735,645 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
    esv3817610mobile element insertion1552estd214human GRCh37 chrX: 126,290,693-126,290,693 , GRCh38.p12 chrX: 127,156,710-127,156,710 0
    esv3817665copy number variation259estd214human GRCh37 chrX: 1,437,891-1,438,937 , GRCh38.p12 chrX: 1,318,998-1,320,044 CSF2RA
    esv3817752copy number variation714estd214human GRCh37 chrX: 53,819,537-53,820,304 , GRCh38.p12 chrX: 53,793,039-53,793,806
    esv3817051copy number variation104estd214human GRCh37 chrX: 125,269,135-125,271,073 , GRCh38.p12 chrX: 126,135,152-126,137,090 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
    esv3817713copy number variation3estd214human GRCh37 chrX: 153,819,664-153,819,664 , GRCh38.p12 chrX: 154,591,401-154,591,401 0
    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
    esv3817829copy number variation603estd214human GRCh37 chrX: 48,500,496-48,502,930 , GRCh38.p12 chrX: 48,642,108-48,644,542 0
    esv3817153copy number variation667estd214human GRCh37 chrX: 53,481,170-53,482,871 , GRCh38.p12 chrX: 53,454,223-53,455,924 TIPINP1
    esv3817661copy number variation1165estd214human GRCh37 chrX: 154,778,170-154,778,667 , GRCh38.p12 chrX: 155,548,509-155,549,006 TMLHE
    esv3817034mobile element insertion242estd214human GRCh37 chrX: 51,693,785-51,693,785 , GRCh38.p12 chrX: 51,950,689-51,950,689 0
    esv3817666copy number variation482estd214human GRCh37 chrX: 70,122,996-70,123,933 , GRCh38.p12 chrX: 70,903,146-70,904,083 TEX11
    esv3817570copy number variation815estd214human GRCh37 chrX: 47,352,939-47,353,908 , GRCh38.p12 chrX: 47,493,540-47,494,509 0
    esv3817158copy number variation1708estd214human GRCh37 chrX: 69,302,587-69,303,799 , GRCh38.p12 chrX: 70,082,737-70,083,949 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