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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968492inversion1nstd209human GRCh38 chr10: 104,554,685-109,812,698 , GRCh37.p13 chr10: 106,314,443-111,572,456 SORCS3, YWHAZP5, 35 more genes
    nsv5501895copy number variation1nstd206human GRCh38 chr10: 108,844,368-108,858,368 , GRCh37.p13 chr10: 110,604,126-110,618,126 MAPKAPK5P1
    nsv5495920copy number variation1nstd206human GRCh38 chr10: 108,847,467-108,847,759 , GRCh37.p13 chr10: 110,607,225-110,607,517 MAPKAPK5P1
    nsv5250950copy number variation1nstd204human GRCh38.p13 chr10: 108,844,152-108,856,713 , GRCh37.p13 chr10: 110,603,910-110,616,471 MAPKAPK5P1
    nsv4974033copy number variation1nstd200human GRCh38 chr10: 108,222,589-109,068,393 , GRCh37.p13 chr10: 109,982,347-110,828,151 MAPKAPK5P1, LOC105378477, 4 more genes
    nsv4970576copy number variation1nstd200human GRCh38 chr10: 108,659,999-109,367,832 , GRCh37.p13 chr10: 110,419,757-111,127,590 RN7SKP278, RNU5B-6P, 3 more genes
    nsv4836218copy number variation1nstd200human GRCh37 chr10: 110,419,757-111,127,590 , GRCh38.p12 chr10: 108,659,999-109,367,832 RNU5B-6P, RNU6-839P, 3 more genes
    nsv4455070copy number variation2nstd102humanUncertain significance GRCh37 chr10: 107,954,392-110,701,910 , GRCh38.p12 chr10: 106,194,634-108,942,152 LINC01435, LOC105378474, 15 more genes
    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
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4179174copy number variation1nstd166human GRCh37.p13 chr10: 110,280,749-110,780,224 , GRCh38.p12 chr10: 108,520,991-109,020,466 RN7SKP278, LINC02661, 1 more genes
    nsv4175757copy number variation1nstd166human GRCh37.p13 chr10: 110,605,000-110,612,400 , GRCh38.p12 chr10: 108,845,242-108,852,642 MAPKAPK5P1
    nsv4175685copy number variation1nstd166human GRCh37.p13 chr10: 110,419,757-111,127,590 , GRCh38.p12 chr10: 108,659,999-109,367,832 MAPKAPK5P1, LINC02661, 3 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3922274copy number variation1nstd102humanUncertain significance NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422 DPCD, LOC105378467, 504 more genes
    nsv3921919copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082 MIR4295, BORCS7, 508 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3919820copy number variation1nstd102humanPathogenic GRCh38 chr10: 107,191,100-118,761,489 , GRCh37 chr10: 108,950,858-120,521,001 , NCBI36 chr10: 108,940,848-120,510,991 CCDC186, RN7SKP288, 147 more genes
    nsv3917744copy number variation1nstd102humanUncertain significance GRCh38 chr10: 108,665,815-109,360,018 , GRCh37 chr10: 110,425,573-111,119,776 , NCBI36 chr10: 110,415,563-111,109,766 MAPKAPK5P1, RNU6-839P, 3 more genes
    nsv3917362copy number variation1nstd102humanUncertain significance NCBI36 chr10: 110,430,646-111,079,711 , GRCh37 chr10: 110,440,656-111,089,721 , GRCh38 chr10: 108,680,898-109,329,963 LINC02661, MAPKAPK5P1, 3 more genes
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