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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7075741inversion1nstd229human GRCh38 chr8: 49,484,248-49,500,738 , GRCh37.p13 chr8: 50,396,807-50,413,297 LOC100507464
    nsv7074141inversion1nstd229human GRCh38 chr8: 48,828,025-51,794,653 , GRCh37.p13 chr8: 49,740,584-52,707,213 CYCSP22, LOC100422267, 19 more genes
    nsv7073972inversion1nstd229human GRCh38 chr8: 49,508,764-49,508,870 , GRCh37.p13 chr8: 50,421,323-50,421,429 LOC100507464
    nsv7073356inversion1nstd229human GRCh38 chr8: 49,484,230-49,503,548 , GRCh37.p13 chr8: 50,396,789-50,416,107 LOC100507464
    nsv6858080copy number variation1nstd229human GRCh38 chr8: 49,493,400-49,659,300 , GRCh37.p13 chr8: 50,405,959-50,571,860 LOC100507464
    nsv6851338copy number variation1nstd229human GRCh38 chr8: 49,446,213-51,704,203 , GRCh37.p13 chr8: 50,358,772-52,616,763 LOC105375828, BRIX1P1, 10 more genes
    nsv6850302copy number variation1nstd229human GRCh38 chr8: 49,374,301-49,619,300 , GRCh37.p13 chr8: 50,286,860-50,531,859 LOC100507464
    nsv6847499copy number variation1nstd229human GRCh38 chr8: 49,482,183-49,500,163 , GRCh37.p13 chr8: 50,394,742-50,412,722 LOC100507464
    nsv6847315copy number variation1nstd229human GRCh38 chr8: 49,490,824-49,501,557 , GRCh37.p13 chr8: 50,403,383-50,414,116 LOC100507464
    nsv6633067copy number variation1nstd224human GRCh37 chr8: 50,306,276-50,505,231 , GRCh38.p12 chr8: 49,393,717-49,592,672 LOC100507464
    nsv6632805copy number variation1nstd224human GRCh37 chr8: 50,412,162-50,528,355 , GRCh38.p12 chr8: 49,499,603-49,615,796 LOC100507464
    nsv6569657inversion1nstd223human GRCh38 chr8: 47,319,822-52,044,550 , GRCh37.p13 chr8: 48,405,007-52,957,110 UBE2V2-AS1, BRIX1P1, 48 more genes
    nsv6427575copy number variation1nstd223human GRCh38 chr8: 49,299,635-51,272,476 , GRCh37.p13 chr8: 50,212,194-52,185,036 CYCSP22, LOC105375830, 10 more genes
    nsv6424740copy number variation1nstd223human GRCh38 chr8: 49,124,516-49,593,471 , GRCh37.p13 chr8: 50,037,075-50,506,030 LOC105375826, LOC100507464, 2 more genes
    nsv6424541copy number variation1nstd223human GRCh38 chr8: 49,493,400-49,659,297 , GRCh37.p13 chr8: 50,405,959-50,571,857 LOC100507464
    nsv6420779copy number variation1nstd223human GRCh38 chr8: 49,510,676-49,511,195 , GRCh37.p13 chr8: 50,423,235-50,423,754 LOC100507464
    nsv6419707copy number variation1nstd223human GRCh38 chr8: 49,509,501-49,511,400 , GRCh37.p13 chr8: 50,422,060-50,423,959 LOC100507464
    nsv6290906copy number variation1nstd102humanLikely benign GRCh37 chr8: 49,923,435-50,560,385 , GRCh38.p12 chr8: 49,010,876-49,647,825 LOC105375826, LOC100507464, 3 more genes
    nsv6290791copy number variation1nstd102humanUncertain significance GRCh37 chr8: 50,208,352-52,190,247 , GRCh38.p12 chr8: 49,295,793-51,277,687 RN7SKP294, LOC105375831, 10 more genes
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