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Items: 1 to 20 of 431

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    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
    nsv7098681copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 99,551,275-101,097,764 , GRCh38.p12 chrX: 100,296,277-101,842,792 TMEM35A, TNMD, 43 more genes
    nsv7090469copy number variation1nstd229human GRCh38 chrX: 101,150,434-101,150,628 , GRCh37.p13 chrX: 100,405,423-100,405,617 CENPI
    nsv7090468copy number variation1nstd229human GRCh38 chrX: 101,112,264-101,112,695 , GRCh37.p13 chrX: 100,367,253-100,367,684 CENPI
    nsv7054248inversion1nstd229human GRCh38 chrX: 101,169,848-101,169,945 , GRCh37.p13 chrX: 100,424,837-100,424,934 CENPI
    nsv7053366inversion1nstd229human GRCh38 chrX: 101,172,843-101,177,674 , GRCh37.p13 chrX: 100,427,832-100,432,663 CENPI
    nsv7049488inversion1nstd229human GRCh38 chrX: 101,169,959-101,169,985 , GRCh37.p13 chrX: 100,424,948-100,424,974 CENPI
    nsv7048731inversion1nstd229human GRCh38 chrX: 101,141,093-101,141,196 , GRCh37.p13 chrX: 100,396,082-100,396,185 CENPI
    nsv7047704inversion1nstd229human GRCh38 chrX: 101,169,880-101,169,955 , GRCh37.p13 chrX: 100,424,869-100,424,944 CENPI
    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
    nsv6636525copy number variation1nstd102humanUncertain significance GRCh37 chrX: 100,118,775-100,510,437 , GRCh38.p12 chrX: 100,863,786-101,255,448 HNRNPA1P27, TMEM35A, 9 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
    nsv6634295copy number variation1nstd224human GRCh37 chrX: 99,957,026-100,400,154 , GRCh38.p12 chrX: 100,702,030-101,145,165 CENPI, TRMT2B, 12 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
    nsv6313391copy number variation1nstd102humanUncertain significance GRCh37 chrX: 99,842,716-100,570,618 , GRCh38.p12 chrX: 100,587,719-101,315,630 RAD21P1, TMEM35A, 19 more genes
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