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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096443copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,781,658-138,665,815 , GRCh38.p12 chr3: 138,062,816-138,946,973 ARMC8, EEF1A1P25, 17 more genes
    nsv7057552inversion1nstd229human GRCh38 chr3: 138,385,643-138,453,260 , GRCh37.p13 chr3: 138,104,485-138,172,102 ESYT3, MRAS
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7042471inversion1nstd229human GRCh38 chr3: 138,157,386-138,843,461 , GRCh37.p13 chr3: 137,876,228-138,562,303 FAIM, DBR1, 10 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv7039034inversion1nstd229human GRCh38 chr3: 136,134,661-138,768,814 , GRCh37.p13 chr3: 135,853,503-138,487,656 KRT8P36, RPL31P23, 37 more genes
    nsv6734851copy number variation1nstd229human GRCh38 chr3: 138,385,601-138,411,300 , GRCh37.p13 chr3: 138,104,443-138,130,142 MRAS
    nsv6730899copy number variation1nstd229human GRCh38 chr3: 138,268,473-138,506,630 , GRCh37.p13 chr3: 137,987,315-138,225,472 CEP70, ARMC8, 3 more genes
    nsv6730439copy number variation1nstd229human GRCh38 chr3: 138,377,522-138,382,537 , GRCh37.p13 chr3: 138,096,364-138,101,379 MRAS
    nsv6724628copy number variation1nstd229human GRCh38 chr3: 138,396,138-138,623,711 , GRCh37.p13 chr3: 138,114,980-138,342,553 CEP70, MRAS, 2 more genes
    nsv6719259copy number variation1nstd229human GRCh38 chr3: 138,357,610-138,362,557 , GRCh37.p13 chr3: 138,076,452-138,081,399 MRAS
    nsv6718739copy number variation1nstd229human GRCh38 chr3: 138,323,101-138,511,200 , GRCh37.p13 chr3: 138,041,943-138,230,042 MRAS, NME9, 2 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6568954inversion1nstd223human GRCh38 chr3: 138,157,386-138,843,464 , GRCh37.p13 chr3: 137,876,228-138,562,306 NME9, FAIM, 10 more genes
    nsv6311953copy number variation1nstd102humanUncertain significance GRCh37 chr3: 138,091,726-138,091,938 , GRCh38.p12 chr3: 138,372,884-138,373,096 MRAS
    nsv6311778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,781,658-139,258,560 , GRCh38.p12 chr3: 138,062,816-139,539,718 PRR23C, ACTG1P1, 29 more genes
    nsv6311440copy number variation1nstd102humanUncertain significance GRCh37 chr3: 138,091,726-138,121,111 , GRCh38.p12 chr3: 138,372,884-138,402,269 MRAS
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    nsv6134409copy number variation1nstd213human GRCh37 chr3: 138,110,000-138,330,001 , GRCh38.p12 chr3: 138,391,158-138,611,159 MRAS, FAIM, 2 more genes
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