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 278

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7091107copy number variation1nstd229human GRCh38 chrX: 138,713,653-138,717,385 , GRCh37.p13 chrX: 137,795,815-137,799,547 FGF13, FGF13-AS1
    nsv7091106copy number variation1nstd229human GRCh38 chrX: 138,712,881-138,713,104 , GRCh37.p13 chrX: 137,795,043-137,795,266 FGF13-AS1, FGF13
    nsv7084459copy number variation1nstd229human GRCh38 chrX: 138,244,796-138,764,581 , GRCh37.p13 chrX: 137,326,955-137,846,743 H2AQ1P, RN7SKP31, 5 more genes
    nsv7084418copy number variation1nstd229human GRCh38 chrX: 137,855,369-139,709,654 , GRCh37.p13 chrX: 136,937,528-138,791,813 FGF13, F9, 10 more genes
    nsv7049576inversion1nstd229human GRCh38 chrX: 138,411,088-139,566,366 , GRCh37.p13 chrX: 137,493,246-138,648,525 MIR504, LOC100130620, 8 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
    nsv6137377copy number variation1nstd213human GRCh37 chrX: 137,740,000-137,850,001 , GRCh38.p12 chrX: 138,657,839-138,767,839 FGF13, MIR504, 1 more genes
    nsv6137376copy number variation1nstd213human GRCh37 chrX: 134,930,000-152,230,001 , GRCh38.p12 chrX: 135,766,029-153,061,271 BCYRN1P1, BRS3, 246 more genes
    nsv6137375copy number variation1nstd213human GRCh37 chrX: 134,920,000-152,230,001 , GRCh38.p12 chrX: 135,751,569-153,061,271 BCYRN1P1, BRS3, 247 more genes
    nsv6137221copy number variation1nstd213human GRCh37 chrX: 66,020,000-152,230,001 , GRCh38.p12 chrX: 66,800,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137215copy number variation3nstd213human GRCh37 chrX: 61,730,000-152,230,001 , GRCh38.p12 chrX: 62,510,530-153,061,271 ABCB7, AGTR2, 1217 more genes
    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