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 441

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7147854insertion1nstd232human GRCh37.p13 chr1: 235,602,236-235,602,236 , GRCh38.p12 chr1: 235,438,921-235,438,921 , GRCh38.p12 chr1|NW_014040927.1: 82,513-82,513 TBCE, B3GALNT2
    nsv7140121insertion1nstd232human GRCh37.p13 chr1: 235,613,660-235,613,660 , GRCh38.p12 chr1: 235,450,345-235,450,345 , GRCh38.p12 chr1|NW_014040927.1: 93,937-93,937 TBCE, B3GALNT2
    nsv7139590insertion1nstd232human GRCh37.p13 chr1: 235,647,833-235,647,833 , GRCh38.p12 chr1: 235,484,517-235,484,517 , GRCh38.p12 chr1|NW_014040927.1: 128,109-128,109 B3GALNT2
    nsv7137173copy number variation1nstd102humanPathogenic GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319 ARID4B, MTND3P8, 58 more genes
    nsv7099266copy number variation1nstd231human GRCh38.p12 chr1: 226,993,371-235,936,592 , GRCh37 chr1: 227,181,072-236,099,892 ACTA1, AGT, 223 more genes
    nsv7095979copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,616,382-235,643,485 , GRCh38.p12 chr1: 235,453,070-235,480,169 , GRCh38.p12 chr1|NW_014040927.1: 96,662-123,761 B3GALNT2
    nsv7095978copy number variation1nstd102humanUncertain significance GRCh37 chr1: 235,611,644-235,612,077 , GRCh38.p12 chr1|NW_014040927.1: 91,921-92,354 , GRCh38.p12 chr1: 235,448,329-235,448,762 B3GALNT2, TBCE
    nsv7095977copy number variation1nstd102humanUncertain significance GRCh37 chr1: 235,543,365-235,619,016 , GRCh38.p12 chr1: 235,380,050-235,455,704 , GRCh38.p12 chr1|NW_014040927.1: 19,851-99,296 TBCE, RPS21P1, 1 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7057850inversion1nstd229human GRCh38 chr1: 235,440,829-235,578,083 , GRCh37.p13 chr1: 235,604,144-235,741,383 MTND6P14, MTND5P19, 8 more genes
    nsv7054147inversion1nstd229human GRCh38 chr1: 235,372,573-235,542,978 , GRCh37.p13 chr1: 235,535,888-235,706,278 MTCO3P46, B3GALNT2, 8 more genes
    nsv7048010inversion1nstd229human GRCh38 chr1: 233,396,223-235,667,657 , GRCh37.p13 chr1: 233,531,969-235,830,957 RN7SL668P, LINC02961, 52 more genes
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv7040505inversion1nstd229human GRCh38 chr1: 235,226,873-236,268,697 , GRCh37.p13 chr1: 235,390,188-236,431,997 RPS21P1, NID1, 26 more genes
    nsv6677097copy number variation1nstd229human GRCh38 chr1: 235,446,148-235,458,163 , GRCh37.p13 chr1: 235,609,463-235,621,471 TBCE, B3GALNT2
    nsv6674321copy number variation1nstd229human GRCh38 chr1: 235,193,806-235,610,253 , GRCh37.p13 chr1: 235,357,121-235,773,553 MTND5P19, RPS21P1, 13 more genes
    nsv6673459copy number variation1nstd229human GRCh38 chr1: 235,405,516-235,553,266 , GRCh37.p13 chr1: 235,568,831-235,716,566 RPS21P1, MTND5P19, 9 more genes
    nsv6671716copy number variation1nstd229human GRCh38 chr1: 235,299,364-235,543,509 , GRCh37.p13 chr1: 235,462,679-235,706,809 B3GALNT2, RPS21P1, 11 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