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 302

    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
    nsv7098547copy number variation1nstd102humanUncertain significance GRCh37 chrX: 71,875,950-71,925,114 , GRCh38.p12 chrX: 72,656,100-72,705,265 MATR3P1, PHKA1, 1 more genes
    nsv7098546copy number variation1nstd102humanUncertain significance GRCh37 chrX: 71,854,985-71,933,728 , GRCh38.p12 chrX: 72,635,135-72,713,880 PHKA1-AS1, MATR3P1, 1 more genes
    nsv7088787copy number variation1nstd229human GRCh38 chrX: 72,707,455-72,707,602 , GRCh37.p13 chrX: 71,927,304-71,927,451 , GRCh37.p13 chrX|NW_004070882.1: 396,472-396,619 PHKA1-AS1, PHKA1
    nsv7088786copy number variation1nstd229human GRCh38 chrX: 72,702,587-72,703,018 , GRCh37.p13 chrX|NW_004070882.1: 391,604-392,035 , GRCh37.p13 chrX: 71,922,437-71,922,868 PHKA1, PHKA1-AS1
    nsv7088785copy number variation1nstd229human GRCh38 chrX: 72,694,839-72,697,432 , GRCh37.p13 chrX|NW_004070882.1: 383,856-386,449 , GRCh37.p13 chrX: 71,914,689-71,917,282 PHKA1, PHKA1-AS1
    nsv7088781copy number variation1nstd229human GRCh38 chrX: 72,672,861-72,741,123 , GRCh37.p13 chrX: 71,892,711-71,960,946 , GRCh37.p13 chrX|NW_004070882.1: 361,878-430,140 PHKA1, RNU1-112P, 2 more genes
    nsv7030865inversion1nstd229human GRCh38 chrX: 72,709,239-72,716,642 , GRCh37.p13 chrX: 71,929,088-71,936,490 , GRCh37.p13 chrX|NW_004070882.1: 398,256-405,659 PHKA1, PHKA1-AS1
    nsv7029251inversion1nstd229human GRCh38 chrX: 72,627,176-72,980,487 , GRCh37.p13 chrX|NW_004070882.1: 316,193-669,504 , GRCh37.p13 chrX: 71,847,026-72,200,323 MATR3P1, DMRTC1B, 11 more genes
    nsv7028785inversion1nstd229human GRCh38 chrX: 72,712,104-72,714,354 , GRCh37.p13 chrX|NW_004070882.1: 401,121-403,371 , GRCh37.p13 chrX: 71,931,946-71,934,202 PHKA1, PHKA1-AS1
    nsv7027327inversion1nstd229human GRCh38 chrX: 72,653,011-73,187,514 , GRCh37.p13 chrX|NW_004070882.1: 342,028-835,911 , GRCh37.p13 chrX: 71,872,861-72,366,730 FAM226A, PABPC1L2B-AS1, 16 more genes
    nsv7018592inversion1nstd229human GRCh38 chrX: 71,642,458-75,115,067 , GRCh37.p13 chrX: 70,862,308-74,334,902 RN7SL648P, LOC101059915, 83 more genes
    nsv6636856copy number variation1nstd102humanUncertain significance GRCh37 chrX: 71,605,731-71,917,944 , GRCh38.p12 chrX: 72,385,881-72,698,094 PHKA1, PHKA1-AS1, 2 more genes
    nsv6636235copy number variation1nstd102humanUncertain significance GRCh37 chrX: 71,605,095-71,917,944 , GRCh38.p12 chrX: 72,385,245-72,698,094 PHKA1-AS1, MATR3P1, 2 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