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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6647144copy number variation1nstd229human GRCh38 chr1: 20,147,364-20,148,724 , GRCh37.p13 chr1: 20,473,857-20,475,217 PLA2G2F
    nsv6647143copy number variation1nstd229human GRCh38 chr1: 20,139,183-20,139,281 , GRCh37.p13 chr1: 20,465,676-20,465,774 PLA2G2F
    nsv6647056copy number variation1nstd229human GRCh38 chr1: 20,140,977-20,145,769 , GRCh37.p13 chr1: 20,467,470-20,472,262 PLA2G2F
    nsv6646976copy number variation1nstd229human GRCh38 chr1: 20,148,070-20,151,541 , GRCh37.p13 chr1: 20,474,563-20,478,034 PLA2G2F
    nsv6646975copy number variation1nstd229human GRCh38 chr1: 20,133,443-20,139,094 , GRCh37.p13 chr1: 20,459,936-20,465,587 PLA2G2F
    nsv6646899copy number variation1nstd229human GRCh38 chr1: 19,751,232-20,412,088 , GRCh37.p13 chr1: 20,077,725-20,738,581 LOC105376826, LOC105376823, 17 more genes
    nsv6646830copy number variation1nstd229human GRCh38 chr1: 20,138,901-20,141,274 , GRCh37.p13 chr1: 20,465,394-20,467,767 PLA2G2F
    nsv6321724copy number variation1nstd223human GRCh38 chr1: 20,137,512-20,145,075 , GRCh37.p13 chr1: 20,464,005-20,471,568 PLA2G2F
    nsv6159386copy number variation1nstd214human GRCh38 chr1: 20,149,293-20,149,386 , GRCh37.p13 chr1: 20,475,786-20,475,879 PLA2G2F
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133962copy number variation1nstd213human GRCh37 chr1: 19,870,000-20,530,001 , GRCh38.p12 chr1: 19,543,506-20,203,508 HTR6, NBL1, 18 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
    nsv6133624copy number variation1nstd213human GRCh37 chr1: 20,350,000-20,570,001 , GRCh38.p12 chr1: 20,023,507-20,243,508 PLA2G5, PLA2G2D, 7 more genes
    nsv6133572copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,950,001 , GRCh38.p12 chr1: 16,943,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
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