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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056318inversion1nstd229human GRCh38 chr5: 135,650,847-136,116,847 , GRCh37.p13 chr5: 134,986,536-135,452,536 VTRNA2-1, LECT2, 8 more genes
    nsv6793528copy number variation1nstd229human GRCh38 chr5: 135,954,901-135,958,646 , GRCh37.p13 chr5: 135,290,590-135,294,335 LECT2
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6786231copy number variation1nstd229human GRCh38 chr5: 135,954,705-135,955,214 , GRCh37.p13 chr5: 135,290,394-135,290,903 LECT2
    nsv6636280copy number variation1nstd102humanUncertain significance GRCh37 chr5: 134,524,754-135,283,222 , GRCh38.p12 chr5: 135,189,064-135,947,533 LINC02900, DCANP1, 12 more genes
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv6135646copy number variation1nstd213human GRCh37 chr5: 124,370,000-136,400,001 , GRCh38.p12 chr5: 125,034,307-137,064,312 ACTBP4, ALDH7A1, 181 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135114copy number variation1nstd213human GRCh37 chr5: 133,550,000-135,990,001 , GRCh38.p12 chr5: 134,214,309-136,654,312 CAMLG, IL9, 53 more genes
    nsv5677327mobile element insertion2nstd211human GRCh38 chr5: 135,954,253-135,954,253 , GRCh37.p13 chr5: 135,289,942-135,289,942 LECT2
    nsv5558422sequence alteration1nstd206human GRCh38 chr5: 135,946,807-135,957,251 , GRCh37.p13 chr5: 135,282,496-135,292,940 LECT2
    nsv5454666copy number variation1nstd206human GRCh38 chr5: 135,946,756-135,957,294 , GRCh37.p13 chr5: 135,282,445-135,292,983 LECT2
    nsv5410987mobile element insertion1nstd206human GRCh38 chr5: 135,954,253-135,954,304 , GRCh37.p13 chr5: 135,289,942-135,289,993 LECT2
    nsv5038943inversion1nstd200human GRCh38 chr5: 135,468,456-136,310,303 , GRCh37.p13 chr5: 134,804,146-135,645,991 SMAD5, SMAD5-AS1, 15 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4590163copy number variation1nstd183human GRCh37 chr5: 135,283,016-135,297,617 , GRCh38.p12 chr5: 135,947,327-135,961,928 LECT2
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4396074copy number variation1nstd174human GRCh37 chr5: 135,281,967-135,297,550 , GRCh38.p12 chr5: 135,946,278-135,961,861 LECT2
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