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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099235copy number variation1nstd231human GRCh38.p12 chr1: 154,116,919-155,715,830 , GRCh37 chr1: 154,089,395-155,685,621 ADAR, CHRNB2, 80 more genes
    nsv7057328inversion1nstd229human GRCh38 chr1: 154,938,555-155,849,490 , GRCh37.p13 chr1: 154,911,031-155,819,281 ENTREP3, YY1AP1, 57 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7049493inversion1nstd229human GRCh38 chr1: 155,330,252-155,334,873 , GRCh37.p13 chr1: 155,300,043-155,304,664 ASH1L, RUSC1
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv7039558inversion1nstd229human GRCh38 chr1: 155,298,171-158,468,090 , GRCh37.p13 chr1: 155,267,962-158,437,880 FCRL4, SCARNA4, 121 more genes
    nsv6549694inversion1nstd223human GRCh38 chr1: 155,298,173-158,468,085 , GRCh37.p13 chr1: 155,267,964-158,437,875 ASH1L, GPATCH4, 121 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6133737copy number variation1nstd213human GRCh37 chr1: 153,820,000-155,320,001 , GRCh38.p12 chr1: 153,847,524-155,350,210 GBA1LP, PKLR, 81 more genes
    nsv6133504copy number variation1nstd213human GRCh37 chr1: 154,420,000-155,500,001 , GRCh38.p12 chr1: 154,447,524-155,530,210 EFNA1, GBA1LP, 51 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5217269copy number variation1nstd204human GRCh38.p13 chr1: 155,315,801-155,621,100 , GRCh37.p13 chr1: 155,285,592-155,590,891 DAP3P1, RNU6-1297P, 13 more genes
    nsv4903915copy number variation1nstd200human GRCh38 chr1: 155,328,653-155,329,168 , GRCh37.p13 chr1: 155,298,444-155,298,959 RUSC1
    nsv4784302copy number variation1nstd200human GRCh37 chr1: 155,298,666-155,299,125 , GRCh38.p12 chr1: 155,328,875-155,329,334 RUSC1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4454226copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,294,636-155,452,240 , GRCh38 chr1: 155,324,845-155,482,449 RUSC1, ASH1L, 4 more genes
    nsv4451749copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,252,202-155,293,625 , GRCh38 chr1: 155,282,411-155,323,834 FDPS, HCN3, 3 more genes
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