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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6829920copy number variation1nstd229human GRCh38 chr7: 88,299,866-88,305,398 , GRCh37.p13 chr7: 87,929,181-87,934,713 STEAP4
    nsv6827918copy number variation1nstd229human GRCh38 chr7: 88,277,832-88,277,977 , GRCh37.p13 chr7: 87,907,147-87,907,292 STEAP4
    nsv6825074copy number variation1nstd229human GRCh38 chr7: 88,267,909-88,292,091 , GRCh37.p13 chr7: 87,897,224-87,921,406 STEAP4
    nsv6824533copy number variation1nstd229human GRCh38 chr7: 88,102,895-88,544,052 , GRCh37.p13 chr7: 87,732,210-88,173,367 LOC100419447, STEAP4, 7 more genes
    nsv6822056copy number variation1nstd229human GRCh38 chr7: 88,288,303-88,358,437 , GRCh37.p13 chr7: 87,917,618-87,987,752 LOC107986815, STEAP4
    nsv6818739copy number variation1nstd229human GRCh38 chr7: 84,598,855-91,861,148 , GRCh37.p13 chr7: 84,228,171-91,490,462 CDK14, LOC101409256, 59 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
    nsv6614093copy number variation1nstd223human GRCh38 chr7: 88,299,866-88,305,394 , GRCh37.p13 chr7: 87,929,181-87,934,709 STEAP4
    nsv6602351copy number variation1nstd223human GRCh38 chr7: 88,283,806-88,284,302 , GRCh37.p13 chr7: 87,913,121-87,913,617 STEAP4
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6313517copy number variation1nstd102humanUncertain significance GRCh37 chr7: 87,733,696-88,171,508 , GRCh38.p12 chr7: 88,104,381-88,542,193 STEAP4, LOC107986815, 7 more genes
    nsv6245551mobile element insertion1nstd215human GRCh38 chr7: 88,270,358-88,270,358 , GRCh37.p13 chr7: 87,899,673-87,899,673 STEAP4
    nsv6137018copy number variation1nstd213human GRCh37 chr7: 87,590,000-88,020,001 , GRCh38.p12 chr7: 87,960,685-88,390,686 SRI, ADAM22, 4 more genes
    nsv6136262copy number variation1nstd213human GRCh37 chr7: 77,010,000-90,950,001 , GRCh38.p12 chr7: 77,380,683-91,320,686 , GRM3, 118 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv5977915inversion1nstd209human GRCh38 chr7: 86,525,777-88,855,329 , GRCh37.p13 chr7: 86,155,093-88,484,643 , GRM3, 31 more genes
    nsv5973961inversion1nstd209human GRCh37.p13 chr7: 87,707,926-88,185,252 , GRCh38 chr7: 88,078,611-88,555,937 SRI, ADAM22, 7 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
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