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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099184copy number variation1nstd231human GRCh38.p12 chr1: 21,486,574-23,087,716 , GRCh37 chr1: 21,813,067-23,414,209 ALPL, C1QA, 36 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
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv6647458copy number variation1nstd229human GRCh38 chr1: 22,658,913-22,658,950 , GRCh37.p13 chr1: 22,985,406-22,985,443 C1QB
    nsv6647457copy number variation1nstd229human GRCh38 chr1: 22,622,346-22,708,970 , GRCh37.p13 chr1: 22,948,839-23,035,463 C1QA, C1QB, 3 more genes
    nsv6647388copy number variation1nstd229human GRCh38 chr1: 22,619,472-22,689,489 , GRCh37.p13 chr1: 22,945,965-23,015,982 C1QA, MIR6127, 2 more genes
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6328775copy number variation1nstd223human GRCh38 chr1: 22,587,296-22,671,210 , GRCh37.p13 chr1: 22,913,789-22,997,703 MIR6127, C1QB, 3 more genes
    nsv6152597copy number variation1nstd214human GRCh38 chr1: 22,659,292-22,659,349 , GRCh37.p13 chr1: 22,985,785-22,985,842 C1QB
    nsv6152056copy number variation1nstd214human GRCh38 chr1: 22,659,292-22,659,353 , GRCh37.p13 chr1: 22,985,785-22,985,846 C1QB
    nsv6151295copy number variation1nstd214human GRCh38 chr1: 22,659,285-22,659,338 , GRCh37.p13 chr1: 22,985,778-22,985,831 C1QB
    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
    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
    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
    nsv6045037insertion1nstd212human GRCh38 chr1: 22,659,222-22,659,222 , GRCh37.p13 chr1: 22,985,715-22,985,715 C1QB
    nsv5982834copy number variation1nstd212human GRCh38 chr1: 22,659,287-22,659,342 , GRCh37.p13 chr1: 22,985,780-22,985,835 C1QB
    nsv5568766copy number variation1nstd207human GRCh38 chr1: 22,659,285-22,659,338 , GRCh37.p13 chr1: 22,985,778-22,985,831 C1QB
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