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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4835491copy number variation1nstd200human GRCh37 chr10: 77,159,527-77,159,694 , GRCh38.p12 chr10: 75,399,769-75,399,936 ZNF503, ZNF503-AS2
    nsv4429611copy number variation1nstd174human GRCh37 chr10: 77,125,891-77,178,843 , GRCh38.p12 chr10: 75,366,133-75,419,085 SPA17P1, ZNF503-AS2, 2 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 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
    nsv4179815copy number variation1nstd166human GRCh37.p13 chr10: 77,161,228-77,161,311 , GRCh38.p12 chr10: 75,401,470-75,401,553 ZNF503, ZNF503-AS2
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
    nsv3910545copy number variation1nstd102humanPathogenic NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132 CAMK2G, MCU, 73 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3905190copy number variation1nstd102humanPathogenic GRCh37 chr10: 75,542,067-79,428,995 , GRCh38.p12 chr10: 73,782,309-77,669,237 TIMM9P1, KCNMA1-AS2, 47 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3895207copy number variation1nstd102humanUncertain significance GRCh37 chr10: 77,158,059-77,272,227 , GRCh38.p12 chr10: 75,398,301-75,512,469 ZNF503-AS2, LOC107984293, 3 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3891070copy number variation1nstd102humanPathogenic GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236 NRG3-AS1, FAM32CP, 441 more genes
    nsv3876996copy number variation1nstd102humanUncertain significance NCBI36 chr10: 75,769,258-77,642,312 , GRCh37.p13 chr10: 76,099,252-77,972,306 , GRCh38.p12 chr10: 74,339,494-76,212,548 MIR606, DUSP29, 27 more genes
    nsv3168535copy number variation1nstd158human GRCh37 chr10: 75,990,986-126,578,233 , GRCh38.p12 chr10: 74,231,228-124,889,664 , ACADSB, 858 more genes
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