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 306

    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
    nsv7090635copy number variation1nstd229human GRCh38 chrX: 103,630,626-103,632,440 , GRCh37.p13 chrX: 102,885,554-102,887,368 TCEAL1
    nsv7090634copy number variation1nstd229human GRCh38 chrX: 103,628,181-103,628,237 , GRCh37.p13 chrX: 102,883,109-102,883,165 TCEAL1
    nsv7090633copy number variation1nstd229human GRCh38 chrX: 103,627,594-103,627,929 , GRCh37.p13 chrX: 102,882,522-102,882,857 TCEAL1
    nsv7090625copy number variation1nstd229human GRCh38 chrX: 103,524,125-103,648,454 , GRCh37.p13 chrX: 102,779,053-102,903,382 LINC02589, TCEAL3, 2 more genes
    nsv7090591copy number variation1nstd229human GRCh38 chrX: 103,123,688-103,793,886 , GRCh37.p13 chrX: 102,378,616-103,048,815 TMEM31, LL0XNC01-250H12.3, 20 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
    nsv6636498copy number variation1nstd102humanUncertain significance GRCh37 chrX: 102,625,535-103,022,965 , GRCh38.p12 chrX: 103,370,607-103,768,037 TCEAL4, TMEM31, 10 more genes
    nsv6636384copy number variation1nstd102humanUncertain significance GRCh37 chrX: 102,615,980-102,962,669 , GRCh38.p12 chrX: 103,361,052-103,707,741 GLRA4, TCEAL4, 9 more genes
    nsv6634595copy number variation1nstd102humanPathogenic GRCh38 chrX: 103,477,300-104,817,980 , GRCh37.p13 chrX: 102,732,228-104,062,660 TMSB15B, MORF4L2-AS1, 33 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
    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
    nsv6315141copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 102,879,326-102,893,312 , GRCh38.p12 chrX: 103,624,398-103,638,384 TCEAL1
    nsv6315111copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 102,774,750-102,929,222 , GRCh38.p12 chrX: 103,519,822-103,674,294 TCEAL1, MORF4L2, 5 more genes
    nsv6313301copy number variation1nstd102humanPathogenic GRCh37 chrX: 101,982,475-116,885,339 , GRCh38.p12 chrX: 102,727,547-117,751,376 TMSB15B, GLUD1P9, 207 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