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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309445copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,250,360-67,254,666 , GRCh38.p12 chr11: 67,482,889-67,487,195 AIP
    nsv7094009copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,250,360-67,250,738 , GRCh38.p12 chr11: 67,482,889-67,483,267 AIP
    nsv3879892copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,249,418-67,255,234 , GRCh38 chr11: 67,481,947-67,487,763 AIP
    nsv4684092copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,253,423-67,254,984 , GRCh38 chr11: 67,485,952-67,487,513 AIP
    nsv3921579delins1nstd102humanLikely pathogenic GRCh37 chr11: 67,250,703-67,250,710 , GRCh38 chr11: 67,483,232-67,483,239 AIP
    nsv3886636copy number variation1nstd102humanLikely benign GRCh37 chr3: 65,609,952-65,661,896 , GRCh38.p12 chr3: 65,624,277-65,676,221 MAGI1
    nsv3886166copy number variation1nstd102humanBenign GRCh37 chr3: 65,796,628-65,817,691 , GRCh38.p12 chr3: 65,810,953-65,832,016 MAGI1
    nsv3893649copy number variation1nstd102humanBenign GRCh37 chr7: 77,767,434-77,776,110 , GRCh38.p12 chr7: 78,138,117-78,146,793 MAGI2
    nsv3888009copy number variation1nstd102humanBenign GRCh37 chr3: 65,802,421-65,804,583 , GRCh38.p12 chr3: 65,816,746-65,818,908 MAGI1
    nsv3904122copy number variation1nstd102humanBenign GRCh37 chr7: 77,672,995-77,916,282 , GRCh38.p12 chr7: 78,043,678-78,286,965 MAGI2
    nsv3922485copy number variation1nstd102humanLikely benign NCBI36 chr3: 65,497,070-65,543,559 , GRCh37 chr3: 65,522,030-65,568,519 , GRCh38 chr3: 65,536,355-65,582,844 MAGI1
    nsv5380728copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,254,459-67,254,666 , GRCh38.p12 chr11: 67,486,988-67,487,195 AIP
    nsv7094010copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,250,630-67,250,738 , GRCh38.p12 chr11: 67,483,159-67,483,267 AIP
    nsv6638082insertion1nstd102humanUncertain significance GRCh37 chr7: 78,997,174-78,997,174 , GRCh38 chr7: 79,367,858-79,367,858 MAGI2
    nsv3887866copy number variation1nstd102humanBenign GRCh37 chr3: 65,969,410-66,101,934 , GRCh38.p12 chr3: 65,983,735-66,116,259 , GRCh38.p12 chr3|NW_012132916.1: 1-93,059 LOC105377128, MAGI1
    nsv3897495copy number variation1nstd102humanBenign GRCh37 chr7: 78,805,941-78,869,490 , GRCh38.p12 chr7: 79,176,625-79,240,174 LOC105375366, MAGI2
    nsv3893090copy number variation1nstd102humanBenign GRCh37 chr7: 78,072,972-78,118,995 , GRCh38.p12 chr7: 78,443,655-78,489,678 MAGI2, UFC1P1
    nsv3893862copy number variation1nstd102humanBenign GRCh37 chr7: 78,095,241-78,118,995 , GRCh38.p12 chr7: 78,465,924-78,489,678 MAGI2, UFC1P1
    nsv4728811copy number variation1nstd102humanUncertain significance GRCh37 chr7: 78,082,858-78,237,175 , GRCh38.p12 chr7: 78,453,541-78,607,858 MAGI2, UFC1P1
    nsv7097756copy number variation1nstd102humanUncertain significance GRCh37 chr7: 77,648,632-77,998,550 , GRCh38.p12 chr7: 78,019,315-78,369,233 MAGI2, RPL13AP17
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