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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
    nsv7090624copy number variation1nstd229human GRCh38 chrX: 103,506,651-103,507,884 , GRCh37.p13 chrX: 102,761,579-102,762,812 LL0XNC01-250H12.3, RAB40A
    nsv7090623copy number variation1nstd229human GRCh38 chrX: 103,498,218-103,500,858 , GRCh37.p13 chrX: 102,753,146-102,755,786 LL0XNC01-250H12.3, RAB40A
    nsv7090622copy number variation1nstd229human GRCh38 chrX: 103,491,901-103,510,100 , GRCh37.p13 chrX: 102,746,829-102,765,028 RAB40A, LL0XNC01-250H12.3
    nsv7090606copy number variation1nstd229human GRCh38 chrX: 103,328,117-103,607,524 , GRCh37.p13 chrX: 102,583,045-102,862,452 TCEAL3, TCEAL9, 6 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
    nsv7051965inversion1nstd229human GRCh38 chrX: 103,505,016-103,505,101 , GRCh37.p13 chrX: 102,759,944-102,760,029 RAB40A, LL0XNC01-250H12.3
    nsv7043677inversion1nstd229human GRCh38 chrX: 103,386,577-103,532,157 , GRCh37.p13 chrX: 102,641,505-102,787,085 RAB40A, LINC02589, 1 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
    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
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