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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7044417inversion1nstd229human GRCh38 chr2: 121,729,048-121,785,423 , GRCh37.p13 chr2: 122,486,624-122,542,999 TSN, NIFK, 2 more genes
    nsv6692432copy number variation1nstd229human GRCh38 chr2: 121,655,001-121,856,100 , GRCh37.p13 chr2: 122,412,577-122,613,676 LOC105373590, RPL12P15, 5 more genes
    nsv6692050copy number variation1nstd229human GRCh38 chr2: 121,452,668-121,789,769 , GRCh37.p13 chr2: 122,210,244-122,547,345 RPL12P15, CLASP1-AS1, 8 more genes
    nsv6691312copy number variation1nstd229human GRCh38 chr2: 121,687,201-121,777,200 , GRCh37.p13 chr2: 122,444,777-122,534,776 NPM1P32, LOC105373590, 3 more genes
    nsv6637021copy number variation1nstd102humanPathogenic GRCh37 chr2: 121,241,775-126,487,783 , GRCh38.p12 chr2: 120,484,199-125,730,206 LOC105373590, LOC105373587, 32 more genes
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6350809copy number variation1nstd223human GRCh38 chr2: 121,419,207-121,790,649 , GRCh37.p13 chr2: 122,176,783-122,548,225 LINC01823, CLASP1, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315168copy number variation1nstd102humanPathogenic GRCh37 chr2: 120,628,484-127,658,188 , GRCh38.p12 chr2: 119,870,908-126,900,612 TSN, LOC107985817, 58 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6134420copy number variation1nstd213human GRCh37 chr2: 117,140,000-144,230,001 , GRCh38.p12 chr2: 116,382,424-143,472,432 BIN1, CCNT2, 382 more genes
    nsv5903293copy number variation1nstd209human GRCh38 chr2: 121,734,749-121,734,806 , GRCh37.p13 chr2: 122,492,325-122,492,382 NIFK
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436164copy number variation1nstd206human GRCh38 chr2: 121,734,750-121,734,807 , GRCh37.p13 chr2: 122,492,326-122,492,383 NIFK
    nsv5435862copy number variation1nstd206human GRCh38 chr2: 121,558,631-122,131,082 , GRCh37.p13 chr2: 122,316,207-122,888,658 TSN, CLASP1, 7 more genes
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