U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 407

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098670copy number variation1nstd102humanUncertain significance GRCh37 chrX: 62,857,908-64,196,257 , GRCh38.p12 chrX: 63,638,028-64,976,377 ZC4H2, LOC100419786, 17 more genes
    nsv7098542copy number variation1nstd102humanPathogenic GRCh37 chrX: 64,196,185-64,196,257 , GRCh38.p12 chrX: 64,976,305-64,976,377 ZC4H2
    nsv7092367copy number variation1nstd229human GRCh38 chrX: 65,022,282-65,022,319 , GRCh37.p13 chrX: 64,242,162-64,242,199 ZC4H2
    nsv7092366copy number variation1nstd229human GRCh38 chrX: 65,020,935-65,021,773 , GRCh37.p13 chrX: 64,240,815-64,241,653 ZC4H2
    nsv7092365copy number variation1nstd229human GRCh38 chrX: 65,014,752-65,018,482 , GRCh37.p13 chrX: 64,234,632-64,238,362 ZC4H2
    nsv7092364copy number variation1nstd229human GRCh38 chrX: 64,983,862-65,000,473 , GRCh37.p13 chrX: 64,203,742-64,220,353 ZC4H2
    nsv7092363copy number variation1nstd229human GRCh38 chrX: 64,983,118-65,020,358 , GRCh37.p13 chrX: 64,202,998-64,240,238 ZC4H2
    nsv7092362copy number variation1nstd229human GRCh38 chrX: 64,977,014-64,980,382 , GRCh37.p13 chrX: 64,196,894-64,200,262 ZC4H2
    nsv7092361copy number variation1nstd229human GRCh38 chrX: 64,976,230-64,976,282 , GRCh37.p13 chrX: 64,196,110-64,196,162 ZC4H2
    nsv7092360copy number variation1nstd229human GRCh38 chrX: 64,952,712-64,954,401 , GRCh37.p13 chrX: 64,172,592-64,174,281 ZC4H2
    nsv7092359copy number variation1nstd229human GRCh38 chrX: 64,943,701-64,946,700 , GRCh37.p13 chrX: 64,163,581-64,166,580 ZC4H2
    nsv7092358copy number variation1nstd229human GRCh38 chrX: 64,943,101-64,946,100 , GRCh37.p13 chrX: 64,162,981-64,165,980 ZC4H2
    nsv7092357copy number variation1nstd229human GRCh38 chrX: 64,941,093-64,943,665 , GRCh37.p13 chrX: 64,160,973-64,163,545 ZC4H2
    nsv7092356copy number variation1nstd229human GRCh38 chrX: 64,938,501-64,946,200 , GRCh37.p13 chrX: 64,158,381-64,166,080 ZC4H2
    nsv7092355copy number variation1nstd229human GRCh38 chrX: 64,938,401-64,946,100 , GRCh37.p13 chrX: 64,158,281-64,165,980 ZC4H2
    nsv7092354copy number variation1nstd229human GRCh38 chrX: 64,938,101-64,943,700 , GRCh37.p13 chrX: 64,157,981-64,163,580 ZC4H2
    nsv7092353copy number variation1nstd229human GRCh38 chrX: 64,938,001-64,942,200 , GRCh37.p13 chrX: 64,157,881-64,162,080 ZC4H2
    nsv7092352copy number variation1nstd229human GRCh38 chrX: 64,938,001-64,941,200 , GRCh37.p13 chrX: 64,157,881-64,161,080 ZC4H2
    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