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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5502567copy number variation1nstd206human GRCh38 chr10: 114,959,879-114,971,110 , GRCh37.p13 chr10: 116,719,638-116,730,869 RNU6-1121P, TRUB1
    nsv5500278copy number variation1nstd206human GRCh38 chr10: 114,876,531-115,123,609 , GRCh37.p13 chr10: 116,636,290-116,786,295 ATRNL1, FHIP2A, 6 more genes
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5315881copy number variation1nstd204human GRCh37.p13 chr10: 116,719,614-116,730,892 , GRCh38.p13 chr10: 114,959,855-114,971,133 RNU6-1121P, TRUB1
    nsv5241212copy number variation1nstd204human GRCh38.p13 chr10: 114,959,901-114,971,100 , GRCh37.p13 chr10: 116,719,660-116,730,859 RNU6-1121P, TRUB1
    nsv5241013copy number variation1nstd204human GRCh38.p13 chr10: 114,959,886-114,968,838 , GRCh37.p13 chr10: 116,719,645-116,728,597 TRUB1, RNU6-1121P
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4977059copy number variation1nstd200human GRCh38 chr10: 114,959,879-114,971,110 , GRCh37.p13 chr10: 116,719,638-116,730,869 TRUB1, RNU6-1121P
    nsv4880587inversion1nstd200human GRCh37 chr10: 115,288,028-117,482,906 , GRCh38.p12 chr10: 113,528,269-115,723,396 , NHLRC2, 31 more genes
    nsv4836755copy number variation1nstd200human GRCh37 chr10: 116,719,638-116,730,869 , GRCh38.p12 chr10: 114,959,879-114,971,110 RNU6-1121P, TRUB1
    nsv4729572copy number variation1nstd102humanUncertain significance GRCh37 chr10: 116,729,745-116,930,466 , GRCh38.p12 chr10: 114,969,986-115,170,708 LINC02626, ATRNL1, 4 more genes
    nsv4616217copy number variation1nstd183human GRCh37 chr10: 116,643,095-116,879,495 , GRCh38.p12 chr10: 114,883,336-115,119,731 ATRNL1, FHIP2A, 6 more genes
    nsv4606361copy number variation1nstd183human GRCh37 chr10: 116,719,638-116,730,869 , GRCh38.p12 chr10: 114,959,879-114,971,110 RNU6-1121P, TRUB1
    nsv4605038copy number variation1nstd183human GRCh37 chr10: 116,636,672-116,881,739 , GRCh38.p12 chr10: 114,876,913-115,121,975 ATRNL1, FHIP2A, 6 more genes
    nsv4456868copy number variation1nstd102humanUncertain significance GRCh37 chr10: 116,643,681-116,879,228 , GRCh38.p12 chr10: 114,883,922-115,119,464 LOC107984272, TRUB1, 6 more genes
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4425554copy number variation1nstd174human GRCh37 chr10: 116,636,290-116,883,372 , GRCh38.p12 chr10: 114,876,531-115,123,608 ATRNL1, FHIP2A, 6 more genes
    nsv4414043copy number variation1nstd174human GRCh37 chr10: 116,719,520-116,730,869 , GRCh38.p12 chr10: 114,959,761-114,971,110 RNU6-1121P, TRUB1
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4183720copy number variation1nstd166human GRCh37.p13 chr10: 116,030,341-117,443,667 , GRCh38.p12 chr10: 114,270,582-115,684,157 VWA2, AFAP1L2, 14 more genes
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