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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7055098inversion1nstd229human GRCh38 chr7: 101,259,637-101,698,862 , GRCh37.p13 chr7: 100,902,918-101,342,142 COL26A1, RNU6-1104P, 7 more genes
    nsv7040420inversion1nstd229human GRCh38 chr7: 101,445,712-104,173,878 , GRCh37.p13 chr7: 101,088,993-103,814,326 ALKBH4, RPS29P16, 54 more genes
    nsv6837365copy number variation1nstd229human GRCh38 chr7: 101,515,458-101,785,260 , GRCh37.p13 chr7: 101,158,739-101,428,540 LOC107986832, COL26A1, 2 more genes
    nsv6837291copy number variation1nstd229human GRCh38 chr7: 101,501,795-101,704,412 , GRCh37.p13 chr7: 101,145,076-101,347,692 MYL10, LOC107986832, 2 more genes
    nsv6830607copy number variation1nstd229human GRCh38 chr7: 101,629,634-101,636,540 , GRCh37.p13 chr7: 101,272,914-101,279,820 MYL10
    nsv6828076copy number variation1nstd229human GRCh38 chr7: 101,526,138-101,698,760 , GRCh37.p13 chr7: 101,169,419-101,342,040 COL26A1, MYL10, 2 more genes
    nsv6826957copy number variation1nstd229human GRCh38 chr7: 100,918,010-102,186,129 , GRCh37.p13 chr7: 100,515,630-101,718,950 COL26A1, AP1S1, 28 more genes
    nsv6824556copy number variation1nstd229human GRCh38 chr7: 101,591,190-101,649,567 , GRCh37.p13 chr7: 101,234,470-101,292,847 LOC107986832, MYL10
    nsv6822665copy number variation1nstd229human GRCh38 chr7: 101,611,506-101,624,110 , GRCh37.p13 chr7: 101,254,786-101,267,390 MYL10
    nsv6820511copy number variation1nstd229human GRCh38 chr7: 100,411,473-102,072,572 , GRCh37.p13 chr7: 100,009,096-101,715,852 MIR4653, UFSP1, 63 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631800copy number variation1nstd224human GRCh37 chr7: 101,183,108-101,269,613 , GRCh38.p12 chr7: 101,539,827-101,626,333 LINC01007, MYL10, 2 more genes
    nsv6619841copy number variation1nstd223human GRCh38 chr7: 101,627,684-101,632,434 , GRCh37.p13 chr7: 101,270,964-101,275,714 MYL10
    nsv6615002copy number variation1nstd223human GRCh38 chr7: 101,620,432-101,621,334 , GRCh37.p13 chr7: 101,263,712-101,264,614 MYL10
    nsv6610311copy number variation1nstd223human GRCh38 chr7: 101,526,138-101,698,760 , GRCh37.p13 chr7: 101,169,419-101,342,040 MYL10, COL26A1, 2 more genes
    nsv6605214copy number variation1nstd223human GRCh38 chr7: 101,291,401-102,143,126 , GRCh37.p13 chr7: 100,934,682-101,718,950 MYL10, EMSLR, 6 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
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