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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145979insertion1nstd232human GRCh37.p13 chr1: 160,295,442-160,295,442 , GRCh38.p12 chr1: 160,325,652-160,325,652 COPA
    nsv7143514copy number variation1nstd232human GRCh37.p13 chr1: 160,267,228-160,267,344 , GRCh38.p12 chr1: 160,297,438-160,297,554 COPA
    nsv7141908copy number variation1nstd232human GRCh37.p13 chr1: 160,261,718-160,261,799 , GRCh38.p12 chr1: 160,291,928-160,292,009 COPA
    nsv7141709insertion1nstd232human GRCh37.p13 chr1: 160,310,086-160,310,086 , GRCh38.p12 chr1: 160,340,296-160,340,296 COPA
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 more genes
    nsv7095484copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,309,679-160,320,060 , GRCh38.p12 chr1: 160,339,889-160,350,270 NCSTN, COPA
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643330copy number variation1nstd229human GRCh38 chr1: 160,265,701-160,317,400 , GRCh37.p13 chr1: 160,235,491-160,287,190 PEX19, RPSAP18, 3 more genes
    nsv6643243copy number variation1nstd229human GRCh38 chr1: 160,339,129-160,339,176 , GRCh37.p13 chr1: 160,308,919-160,308,966 COPA
    nsv6643242copy number variation1nstd229human GRCh38 chr1: 160,334,691-160,361,661 , GRCh37.p13 chr1: 160,304,481-160,331,451 NCSTN, COPA
    nsv6643239copy number variation1nstd229human GRCh38 chr1: 160,300,627-160,304,539 , GRCh37.p13 chr1: 160,270,417-160,274,329 COPA
    nsv6643125copy number variation1nstd229human GRCh38 chr1: 160,339,105-160,339,177 , GRCh37.p13 chr1: 160,308,895-160,308,967 COPA
    nsv6642901copy number variation1nstd229human GRCh38 chr1: 160,335,401-160,338,200 , GRCh37.p13 chr1: 160,305,191-160,307,990 COPA
    nsv6642899copy number variation1nstd229human GRCh38 chr1: 160,314,346-160,318,802 , GRCh37.p13 chr1: 160,284,136-160,288,592 COPA, SUMO1P3
    nsv6642898copy number variation1nstd229human GRCh38 chr1: 160,310,801-160,318,600 , GRCh37.p13 chr1: 160,280,591-160,288,390 COPA, SUMO1P3
    nsv6642897copy number variation1nstd229human GRCh38 chr1: 160,297,601-160,434,000 , GRCh37.p13 chr1: 160,267,391-160,403,790 LOC105371466, VANGL2, 6 more genes
    nsv6637035copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,778,364-160,770,515 , GRCh38.p12 chr1: 159,808,574-160,800,725 PEX19, SLAMF8, 43 more genes
    nsv6335462copy number variation1nstd223human GRCh38 chr1: 160,300,627-160,304,535 , GRCh37.p13 chr1: 160,270,417-160,274,325 COPA
    nsv6310733copy number variation2nstd102humanUncertain significance GRCh37 chr1: 160,090,676-160,327,063 , GRCh38.p12 chr1: 160,120,886-160,357,273 SUMO1P3, NCSTN, 11 more genes
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