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Items: 1 to 20 of 645

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094181copy number variation1nstd102humanPathogenic GRCh37 chr11: 68,153,764-68,157,540 , GRCh38.p12 chr11: 68,386,296-68,390,072 LRP5
    nsv7094103copy number variation1nstd102humanPathogenic GRCh37 chr11: 68,207,225-68,207,404 , GRCh38.p12 chr11: 68,439,757-68,439,936 LRP5
    nsv7094102copy number variation1nstd102humanPathogenic GRCh37 chr11: 68,131,195-68,131,431 , GRCh38.p12 chr11: 68,363,727-68,363,963 LRP5
    nsv7094101copy number variation1nstd102humanPathogenic GRCh37 chr11: 68,080,076-68,216,744 , GRCh38.p12 chr11: 68,312,608-68,449,276 LRP5
    nsv7094099copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,759,017-68,216,538 , GRCh38.p12 chr11: 67,991,546-68,449,070 LRP5, UNC93B1, 11 more genes
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7094011copy number variation1nstd102humanUncertain significance GRCh37 chr11: 68,197,023-68,458,455 , GRCh38.p12 chr11: 68,429,555-68,690,987 PPP6R3, NDUFA3P2, 3 more genes
    nsv7093942copy number variation1nstd102humanUncertain significance GRCh37 chr11: 68,153,764-68,216,538 , GRCh38.p12 chr11: 68,386,296-68,449,070 LRP5
    nsv7093941copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 68,115,295-68,115,731 , GRCh38.p12 chr11: 68,347,827-68,348,263 LRP5
    nsv7093940copy number variation1nstd102humanPathogenic GRCh37 chr11: 68,080,183-68,080,293 , GRCh38.p12 chr11: 68,312,715-68,312,825 LRP5
    nsv7093493insertion1nstd102humanPathogenic GRCh37 chr11: 68,170,946-68,170,946 , GRCh38 chr11: 68,403,478-68,403,478 LRP5
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7073359inversion1nstd229human GRCh38 chr11: 68,334,639-68,336,763 , GRCh37.p13 chr11: 68,102,107-68,104,231 LRP5
    nsv7068521inversion1nstd229human GRCh38 chr11: 68,233,059-68,759,151 , GRCh37.p13 chr11: 68,000,526-68,526,619 GAL, LOC105369363, 7 more genes
    nsv6918034copy number variation1nstd229human GRCh38 chr11: 68,399,005-68,405,981 , GRCh37.p13 chr11: 68,166,473-68,173,449 LRP5
    nsv6917849copy number variation1nstd229human GRCh38 chr11: 68,326,528-68,335,678 , GRCh37.p13 chr11: 68,093,996-68,103,146 LRP5
    nsv6917224copy number variation1nstd229human GRCh38 chr11: 68,410,779-68,412,896 , GRCh37.p13 chr11: 68,178,247-68,180,364 LRP5
    nsv6916665copy number variation1nstd229human GRCh38 chr11: 68,405,171-68,409,866 , GRCh37.p13 chr11: 68,172,639-68,177,334 LRP5
    nsv6915427copy number variation1nstd229human GRCh38 chr11: 68,316,143-68,320,749 , GRCh37.p13 chr11: 68,083,611-68,088,217 LRP5
    nsv6914188copy number variation1nstd229human GRCh38 chr11: 68,310,963-68,320,284 , GRCh37.p13 chr11: 68,078,431-68,087,752 LRP5
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