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 394

    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
    nsv7098672copy number variation1nstd102humanUncertain significance GRCh37 chrX: 66,905,832-68,060,497 , GRCh38.p12 chrX: 67,685,990-68,840,654 SERBP1P1, COX6CP12, 14 more genes
    nsv7088429copy number variation1nstd229human GRCh38 chrX: 68,571,138-68,571,451 , GRCh37.p13 chrX: 67,790,980-67,791,293 YIPF6
    nsv7088428copy number variation1nstd229human GRCh38 chrX: 68,566,134-68,572,476 , GRCh37.p13 chrX: 67,785,976-67,792,318 YIPF6
    nsv7088427copy number variation1nstd229human GRCh38 chrX: 68,553,779-68,554,667 , GRCh37.p13 chrX: 67,773,621-67,774,509 YIPF6
    nsv7088426copy number variation1nstd229human GRCh38 chrX: 68,553,653-68,554,299 , GRCh37.p13 chrX: 67,773,495-67,774,141 YIPF6
    nsv7088425copy number variation1nstd229human GRCh38 chrX: 68,552,201-68,554,800 , GRCh37.p13 chrX: 67,772,043-67,774,642 YIPF6
    nsv7088424copy number variation1nstd229human GRCh38 chrX: 68,538,662-68,570,015 , GRCh37.p13 chrX: 67,758,504-67,789,857 YIPF6, RNU6-245P
    nsv7088423copy number variation1nstd229human GRCh38 chrX: 68,524,101-68,526,500 , GRCh37.p13 chrX: 67,743,943-67,746,342 YIPF6
    nsv7088422copy number variation1nstd229human GRCh38 chrX: 68,510,601-68,528,800 , GRCh37.p13 chrX: 67,730,443-67,748,642 YIPF6
    nsv7088421copy number variation1nstd229human GRCh38 chrX: 68,502,071-68,761,314 , GRCh37.p13 chrX: 67,721,913-67,981,156 RNU6-245P, YIPF6, 3 more genes
    nsv7088420copy number variation1nstd229human GRCh38 chrX: 68,501,801-68,501,971 , GRCh37.p13 chrX: 67,721,643-67,721,813 YIPF6
    nsv7088406copy number variation1nstd229human GRCh38 chrX: 68,344,301-68,510,900 , GRCh37.p13 chrX: 67,564,143-67,730,742 OPHN1, YIPF6, 1 more genes
    nsv7088372copy number variation1nstd229human GRCh38 chrX: 67,981,787-68,547,691 , GRCh37.p13 chrX: 67,201,629-67,767,533 LOC100128467, PGK1P1, 5 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    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