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Items: 1 to 20 of 957

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099250copy number variation1nstd231human GRCh38.p12 chr1: 174,623,673-177,335,804 , GRCh37 chr1: 174,592,811-177,304,940 ASTN1, TNR, 29 more genes
    nsv7099249copy number variation1nstd231human GRCh38.p12 chr1: 173,922,587-174,397,868 , GRCh37 chr1: 173,891,725-174,367,006 RABGAP1L, RC3H1, 6 more genes
    nsv7098710complex chromosomal rearrangement11nstd230human GRCh37 chr1: 173,965,566-173,965,566 , GRCh37 chr1: 173,965,577-173,965,577 , GRCh37 chr1: 174,535,751-174,535,751 , GRCh37 chr1: 174,535,755-174,535,755 , GRCh37 chr1: 175,372,368-175,372,368 , GRCh37 chr1: 175,372,368-175,372,368 , GRCh37 chr6: 22,852,567-22,852,567 , GRCh37 chr6: 22,852,569-22,852,569 , GRCh37 chr6: 107,302,954-107,302,954 , GRCh37 chr6: 107,752,783-107,752,783 , GRCh37 chr6: 109,359,196-109,359,196 , GRCh37 chr6: 112,693,619-112,693,619 , GRCh37 chr6: 113,465,033-113,465,033 , GRCh37 chr6: 113,465,033-113,465,033 , GRCh37 chr6: 124,991,331-124,991,331 , GRCh37 chr6: 124,991,331-124,991,331 , GRCh37 chr6: 130,542,182-130,542,182 , GRCh37 chr6: 130,542,184-130,542,184 , GRCh37 chr6: 141,922,305-141,922,305 , GRCh37 chr6: 141,922,306-141,922,306 , GRCh37 chr9: 10,071,147-10,071,147 , GRCh37 chr9: 10,071,149-10,071,149 , GRCh38.p12 chr1: 173,996,428-173,996,428 , GRCh38.p12 chr1: 173,996,439-173,996,439 , GRCh38.p12 chr1: 174,566,613-174,566,613 , GRCh38.p12 chr1: 174,566,617-174,566,617 , GRCh38.p12 chr1: 175,403,232-175,403,232 , GRCh38.p12 chr1: 175,403,232-175,403,232 , GRCh38.p12 chr6: 22,852,338-22,852,338 , GRCh38.p12 chr6: 22,852,340-22,852,340 , GRCh38.p12 chr6: 106,855,079-106,855,079 , GRCh38.p12 chr6: 107,431,579-107,431,579 , GRCh38.p12 chr6: 109,037,993-109,037,993 , GRCh38.p12 chr6: 112,372,417-112,372,417 , GRCh38.p12 chr6: 113,143,831-113,143,831 , GRCh38.p12 chr6: 113,143,831-113,143,831 , GRCh38.p12 chr6: 124,670,185-124,670,185 , GRCh38.p12 chr6: 124,670,185-124,670,185 , GRCh38.p12 chr6: 130,221,037-130,221,037 , GRCh38.p12 chr6: 130,221,039-130,221,039 , GRCh38.p12 chr6: 141,601,168-141,601,168 , GRCh38.p12 chr6: 141,601,169-141,601,169 , GRCh38.p12 chr9: 10,071,147-10,071,147 , GRCh38.p12 chr9: 10,071,149-10,071,149 PTPRD, TNR, 6 more genes
    nsv7057894inversion1nstd229human GRCh38 chr1: 174,956,226-174,956,314 , GRCh37.p13 chr1: 174,925,363-174,925,451 RABGAP1L
    nsv7057654inversion1nstd229human GRCh38 chr1: 174,897,019-174,899,380 , GRCh37.p13 chr1: 174,866,156-174,868,517 RABGAP1L
    nsv7057423inversion1nstd229human GRCh38 chr1: 174,504,900-174,504,932 , GRCh37.p13 chr1: 174,474,038-174,474,070 RABGAP1L
    nsv7053278inversion1nstd229human GRCh38 chr1: 174,313,760-174,313,834 , GRCh37.p13 chr1: 174,282,898-174,282,972 RABGAP1L
    nsv7051017inversion1nstd229human GRCh38 chr1: 174,929,658-174,929,919 , GRCh37.p13 chr1: 174,898,795-174,899,056 RABGAP1L
    nsv7048581inversion1nstd229human GRCh38 chr1: 174,019,781-174,476,285 , GRCh37.p13 chr1: 173,988,919-174,445,423 LOC100302291, RC3H1, 6 more genes
    nsv7046006inversion1nstd229human GRCh38 chr1: 174,625,666-174,671,047 , GRCh37.p13 chr1: 174,594,804-174,640,185 RABGAP1L
    nsv7044079inversion1nstd229human GRCh38 chr1: 174,711,171-179,623,233 , GRCh37.p13 chr1: 174,680,309-179,592,368 LOC100420262, RNU6-307P, 71 more genes
    nsv7043887inversion1nstd229human GRCh38 chr1: 174,699,785-174,699,803 , GRCh37.p13 chr1: 174,668,923-174,668,941 RABGAP1L
    nsv7043495inversion1nstd229human GRCh38 chr1: 174,244,589-174,250,612 , GRCh37.p13 chr1: 174,213,727-174,219,750 RABGAP1L
    nsv7042698inversion1nstd229human GRCh38 chr1: 174,264,571-174,264,620 , GRCh37.p13 chr1: 174,233,709-174,233,758 RABGAP1L
    nsv7040104inversion1nstd229human GRCh38 chr1: 174,510,834-174,510,846 , GRCh37.p13 chr1: 174,479,972-174,479,984 RABGAP1L
    nsv6645148copy number variation1nstd229human GRCh38 chr1: 174,968,582-175,319,578 , GRCh37.p13 chr1: 174,937,719-175,288,714 RPS29P4, MRPS14, 9 more genes
    nsv6645147copy number variation1nstd229human GRCh38 chr1: 174,827,422-174,832,711 , GRCh37.p13 chr1: 174,796,560-174,801,849 RABGAP1L
    nsv6645145copy number variation1nstd229human GRCh38 chr1: 174,720,056-174,720,222 , GRCh37.p13 chr1: 174,689,194-174,689,360 RABGAP1L
    nsv6645143copy number variation1nstd229human GRCh38 chr1: 174,671,110-174,672,274 , GRCh37.p13 chr1: 174,640,248-174,641,412 RABGAP1L
    nsv6645142copy number variation1nstd229human GRCh38 chr1: 174,642,401-174,650,900 , GRCh37.p13 chr1: 174,611,539-174,620,038 RABGAP1L
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