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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051208inversion1nstd229human GRCh38 chr7: 108,879,788-112,571,756 , GRCh37.p13 chr7: 108,519,845-112,211,811 LOC100420226, LOC100421901, 25 more genes
    nsv6837454copy number variation1nstd229human GRCh38 chr7: 108,861,373-108,905,433 , GRCh37.p13 chr7: 108,501,817-108,545,490 LINC02903
    nsv6836734copy number variation1nstd229human GRCh38 chr7: 108,718,928-108,911,356 , GRCh37.p13 chr7: 108,359,372-108,551,413 LINC02903, LOC107986836, 1 more genes
    nsv6835700copy number variation1nstd229human GRCh38 chr7: 108,688,733-108,959,840 , GRCh37.p13 chr7: 108,329,177-108,599,897 LOC100419644, LINC02903, 1 more genes
    nsv6834698copy number variation1nstd229human GRCh38 chr7: 108,749,464-109,001,301 , GRCh37.p13 chr7: 108,389,908-108,641,358 BUB3P1, LOC107986836, 1 more genes
    nsv6832850copy number variation1nstd229human GRCh38 chr7: 108,875,364-108,991,126 , GRCh37.p13 chr7: 108,515,421-108,631,183 LINC02903
    nsv6831637copy number variation1nstd229human GRCh38 chr7: 108,749,501-109,001,300 , GRCh37.p13 chr7: 108,389,945-108,641,357 LOC107986836, LINC02903, 1 more genes
    nsv6831625copy number variation1nstd229human GRCh38 chr7: 108,873,399-109,041,302 , GRCh37.p13 chr7: 108,513,456-108,681,359 LINC02903, BUB3P1
    nsv6823681copy number variation1nstd229human GRCh38 chr7: 108,851,270-108,992,959 , GRCh37.p13 chr7: 108,491,714-108,633,016 BUB3P1, LINC02903
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6617125copy number variation1nstd223human GRCh38 chr7: 108,884,588-108,885,203 , GRCh37.p13 chr7: 108,524,645-108,525,260 LINC02903
    nsv6614078copy number variation1nstd223human GRCh38 chr7: 108,688,733-108,959,842 , GRCh37.p13 chr7: 108,329,177-108,599,899 LOC100419644, LOC107986836, 1 more genes
    nsv6611247copy number variation1nstd223human GRCh38 chr7: 108,865,181-109,017,030 , GRCh37.p13 chr7: 108,505,625-108,657,087 LINC02903, BUB3P1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 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
    nsv6136536copy number variation1nstd213human GRCh37 chr7: 107,510,000-112,950,001 , GRCh38.p12 chr7: 107,869,555-113,309,946 NPM1P14, LRRN3, 52 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135948copy number variation1nstd213human GRCh37 chr7: 105,420,000-108,740,001 , GRCh38.p12 chr7: 105,779,554-109,099,944 NAMPT, COG5, 49 more genes
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