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 335

    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
    nsv7078163copy number variation1nstd229human GRCh38 chrX: 105,548,601-105,582,800 , GRCh37.p13 chrX: 104,792,594-104,826,793 LOC107985680, IL1RAPL2
    nsv7078162copy number variation1nstd229human GRCh38 chrX: 105,544,227-105,552,845 , GRCh37.p13 chrX: 104,788,220-104,796,838 LOC107985680, IL1RAPL2
    nsv7078161copy number variation1nstd229human GRCh38 chrX: 105,543,541-105,548,031 , GRCh37.p13 chrX: 104,787,534-104,792,024 IL1RAPL2, LOC107985680
    nsv7078160copy number variation1nstd229human GRCh38 chrX: 105,538,204-105,596,458 , GRCh37.p13 chrX: 104,782,197-104,840,451 LOC107985680, IL1RAPL2
    nsv7078159copy number variation1nstd229human GRCh38 chrX: 105,536,414-105,548,453 , GRCh37.p13 chrX: 104,780,407-104,792,446 LOC107985680, IL1RAPL2
    nsv7078158copy number variation1nstd229human GRCh38 chrX: 105,527,101-105,547,600 , GRCh37.p13 chrX: 104,771,094-104,791,593 IL1RAPL2, LOC107985680
    nsv7078157copy number variation1nstd229human GRCh38 chrX: 105,523,957-105,557,382 , GRCh37.p13 chrX: 104,767,950-104,801,375 IL1RAPL2, LOC107985680
    nsv7078156copy number variation1nstd229human GRCh38 chrX: 105,522,501-105,582,800 , GRCh37.p13 chrX: 104,766,494-104,826,793 IL1RAPL2, LOC107985680
    nsv7078153copy number variation1nstd229human GRCh38 chrX: 105,494,891-105,560,741 , GRCh37.p13 chrX: 104,738,883-104,804,734 IL1RAPL2, LOC107985680
    nsv7078150copy number variation1nstd229human GRCh38 chrX: 105,456,601-105,572,800 , GRCh37.p13 chrX: 104,700,593-104,816,793 LOC107985680, IL1RAPL2
    nsv7078149copy number variation1nstd229human GRCh38 chrX: 105,450,301-105,585,300 , GRCh37.p13 chrX: 104,694,293-104,829,293 LOC107985680, IL1RAPL2
    nsv7078140copy number variation1nstd229human GRCh38 chrX: 105,389,198-105,590,364 , GRCh37.p13 chrX: 104,633,869-104,834,357 IL1RAPL2, LOC107985680, 1 more genes
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7044993inversion1nstd229human GRCh38 chrX: 104,618,913-113,302,073 , GRCh37.p13 chrX: 103,863,594-112,545,300 NCBP2L, TEX13B, 92 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 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
    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