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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6877652copy number variation1nstd229human GRCh38 chr9: 111,313,279-111,325,747 , GRCh37.p13 chr9: 114,075,559-114,088,027 OR2K2
    nsv6876301copy number variation1nstd229human GRCh38 chr9: 111,305,001-111,357,700 , GRCh37.p13 chr9: 114,067,281-114,119,980 OR2K2
    nsv6870282copy number variation1nstd229human GRCh38 chr9: 111,278,081-111,350,645 , GRCh37.p13 chr9: 114,040,361-114,112,925 LOC105376219, OR2K2
    nsv6861011copy number variation1nstd229human GRCh38 chr9: 111,035,445-111,332,237 , GRCh37.p13 chr9: 113,797,725-114,094,517 LPAR1, MIR7702, 3 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6315460copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,673,200-115,935,268 , GRCh38.p12 chr9: 110,910,920-113,172,988 MIR4668, LINC02977, 40 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6137434copy number variation1nstd213human GRCh37 chr9: 113,800,000-114,260,001 , GRCh38.p12 chr9: 111,037,720-111,497,721 LPAR1, ECPAS, 5 more genes
    nsv6136725copy number variation1nstd213human GRCh37 chr9: 113,990,000-114,140,001 , GRCh38.p12 chr9: 111,227,720-111,377,721 ECPAS, OR2K2, 2 more genes
    nsv6136724copy number variation1nstd213human GRCh37 chr9: 113,960,000-114,290,001 , GRCh38.p12 chr9: 111,197,720-111,527,721 ECPAS, OR2K2, 4 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456379copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,982,711-117,443,628 , GRCh38.p12 chr9: 111,220,431-114,681,348 MIR4668, LOC100418705, 74 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4183371copy number variation1nstd166human GRCh37.p13 chr9: 114,072,322-114,413,126 , GRCh38.p12 chr9: 111,310,042-111,650,846 PTGR1, ECPAS, 7 more genes
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 more genes
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