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 1009

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147332copy number variation1nstd232human GRCh37.p13 chr1: 175,516,705-175,516,756 , GRCh38.p12 chr1: 175,547,569-175,547,620 TNR
    nsv7140480copy number variation1nstd232human GRCh37.p13 chr1: 175,395,974-175,396,087 , GRCh38.p12 chr1: 175,426,838-175,426,951 TNR
    nsv7099250copy number variation1nstd231human GRCh38.p12 chr1: 174,623,673-177,335,804 , GRCh37 chr1: 174,592,811-177,304,940 ASTN1, TNR, 29 more genes
    nsv7098710complex chromosomal rearrangement11nstd230human GRCh37 chr1: 173,965,566-173,965,566 , GRCh37 chr1: 173,965,577-173,965,577 , GRCh37 chr1: 174,535,751-174,535,751 , GRCh37 chr1: 174,535,755-174,535,755 , GRCh37 chr1: 175,372,368-175,372,368 , GRCh37 chr1: 175,372,368-175,372,368 , GRCh37 chr6: 22,852,567-22,852,567 , GRCh37 chr6: 22,852,569-22,852,569 , GRCh37 chr6: 107,302,954-107,302,954 , GRCh37 chr6: 107,752,783-107,752,783 , GRCh37 chr6: 109,359,196-109,359,196 , GRCh37 chr6: 112,693,619-112,693,619 , GRCh37 chr6: 113,465,033-113,465,033 , GRCh37 chr6: 113,465,033-113,465,033 , GRCh37 chr6: 124,991,331-124,991,331 , GRCh37 chr6: 124,991,331-124,991,331 , GRCh37 chr6: 130,542,182-130,542,182 , GRCh37 chr6: 130,542,184-130,542,184 , GRCh37 chr6: 141,922,305-141,922,305 , GRCh37 chr6: 141,922,306-141,922,306 , GRCh37 chr9: 10,071,147-10,071,147 , GRCh37 chr9: 10,071,149-10,071,149 , GRCh38.p12 chr1: 173,996,428-173,996,428 , GRCh38.p12 chr1: 173,996,439-173,996,439 , GRCh38.p12 chr1: 174,566,613-174,566,613 , GRCh38.p12 chr1: 174,566,617-174,566,617 , GRCh38.p12 chr1: 175,403,232-175,403,232 , GRCh38.p12 chr1: 175,403,232-175,403,232 , GRCh38.p12 chr6: 22,852,338-22,852,338 , GRCh38.p12 chr6: 22,852,340-22,852,340 , GRCh38.p12 chr6: 106,855,079-106,855,079 , GRCh38.p12 chr6: 107,431,579-107,431,579 , GRCh38.p12 chr6: 109,037,993-109,037,993 , GRCh38.p12 chr6: 112,372,417-112,372,417 , GRCh38.p12 chr6: 113,143,831-113,143,831 , GRCh38.p12 chr6: 113,143,831-113,143,831 , GRCh38.p12 chr6: 124,670,185-124,670,185 , GRCh38.p12 chr6: 124,670,185-124,670,185 , GRCh38.p12 chr6: 130,221,037-130,221,037 , GRCh38.p12 chr6: 130,221,039-130,221,039 , GRCh38.p12 chr6: 141,601,168-141,601,168 , GRCh38.p12 chr6: 141,601,169-141,601,169 , GRCh38.p12 chr9: 10,071,147-10,071,147 , GRCh38.p12 chr9: 10,071,149-10,071,149 PTPRD, TNR, 6 more genes
    nsv7055583inversion1nstd229human GRCh38 chr1: 175,495,551-175,495,583 , GRCh37.p13 chr1: 175,464,687-175,464,719 TNR
    nsv7051567inversion1nstd229human GRCh38 chr1: 175,730,873-175,737,542 , GRCh37.p13 chr1: 175,700,009-175,706,678 TNR
    nsv7045375inversion1nstd229human GRCh38 chr1: 175,580,636-175,589,524 , GRCh37.p13 chr1: 175,549,772-175,558,660 TNR
    nsv7044079inversion1nstd229human GRCh38 chr1: 174,711,171-179,623,233 , GRCh37.p13 chr1: 174,680,309-179,592,368 LOC100420262, RNU6-307P, 71 more genes
    nsv7041598inversion1nstd229human GRCh38 chr1: 175,417,768-175,422,700 , GRCh37.p13 chr1: 175,386,904-175,391,836 TNR
    nsv6645169copy number variation1nstd229human GRCh38 chr1: 175,736,801-175,740,100 , GRCh37.p13 chr1: 175,705,937-175,709,236 TNR
    nsv6645167copy number variation1nstd229human GRCh38 chr1: 175,561,535-175,565,139 , GRCh37.p13 chr1: 175,530,671-175,534,275 TNR
    nsv6645166copy number variation1nstd229human GRCh38 chr1: 175,534,164-175,546,156 , GRCh37.p13 chr1: 175,503,300-175,515,292 TNR
    nsv6645165copy number variation1nstd229human GRCh38 chr1: 175,473,313-175,479,139 , GRCh37.p13 chr1: 175,442,449-175,448,275 TNR
    nsv6645164copy number variation1nstd229human GRCh38 chr1: 175,469,761-175,474,866 , GRCh37.p13 chr1: 175,438,897-175,444,002 TNR
    nsv6645163copy number variation1nstd229human GRCh38 chr1: 175,460,980-175,792,704 , GRCh37.p13 chr1: 175,430,116-175,761,840 TNR
    nsv6645161copy number variation1nstd229human GRCh38 chr1: 175,393,901-175,396,800 , GRCh37.p13 chr1: 175,363,037-175,365,936 TNR
    nsv6645160copy number variation1nstd229human GRCh38 chr1: 175,372,886-175,376,007 , GRCh37.p13 chr1: 175,342,022-175,345,143 TNR
    nsv6645159copy number variation1nstd229human GRCh38 chr1: 175,370,479-175,373,557 , GRCh37.p13 chr1: 175,339,615-175,342,693 TNR
    nsv6645156copy number variation1nstd229human GRCh38 chr1: 175,276,901-175,371,400 , GRCh37.p13 chr1: 175,246,037-175,340,536 LOC105371623, TNR, 1 more genes
    nsv6645148copy number variation1nstd229human GRCh38 chr1: 174,968,582-175,319,578 , GRCh37.p13 chr1: 174,937,719-175,288,714 RPS29P4, MRPS14, 9 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