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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148184copy number variation1nstd102humanPathogenic GRCh38 chr1: 243,221,458-248,919,110 , GRCh37.p13 chr1: 243,384,760-249,213,309 LOC105373271, LOC107985725, 153 more genes
    nsv7099272copy number variation1nstd231human GRCh38.p12 chr1: 243,197,153-248,437,482 , GRCh37 chr1: 243,360,455-248,600,783 ADSS2, HNRNPU, 124 more genes
    nsv7098854copy number variation1nstd102humanPathogenic GRCh37 chr1: 245,704,069-249,212,562 , GRCh38.p12 chr1: 245,540,767-248,918,363 OR2X1P, OR14A2, 118 more genes
    nsv7055426inversion1nstd229human GRCh38 chr1: 247,429,281-247,845,194 , GRCh37.p13 chr1: 247,592,583-248,008,496 OR14L1, OR6R1P, 19 more genes
    nsv7051894inversion1nstd229human GRCh38 chr1: 245,875,322-247,636,891 , GRCh37.p13 chr1: 246,038,624-247,800,193 NLRP3, LOC105373273, 46 more genes
    nsv7049548inversion1nstd229human GRCh38 chr1: 247,434,792-247,854,366 , GRCh37.p13 chr1: 247,598,094-248,017,668 OR2G2, LOC102724446, 19 more genes
    nsv7043773inversion1nstd229human GRCh38 chr1: 247,051,888-247,648,554 , GRCh37.p13 chr1: 247,215,190-247,811,856 OR2C3, ZNF496, 27 more genes
    nsv7043050inversion1nstd229human GRCh38 chr1: 246,982,942-247,630,602 , GRCh37.p13 chr1: 247,146,244-247,793,904 LOC100419806, GCSAML-AS1, 30 more genes
    nsv7041671inversion1nstd229human GRCh38 chr1: 247,239,306-248,299,501 , GRCh37.p13 chr1: 247,402,608-248,462,803 OR9H1P, OR2L9P, 49 more genes
    nsv7040948inversion1nstd229human GRCh38 chr1: 247,397,103-247,762,133 , GRCh37.p13 chr1: 247,560,405-247,925,435 OR2G3, OR2W5P, 14 more genes
    nsv6673925copy number variation1nstd229human GRCh38 chr1: 247,506,357-247,841,446 , GRCh37.p13 chr1: 247,669,659-248,004,748 OR14A2, OR14L1, 16 more genes
    nsv6671063copy number variation1nstd229human GRCh38 chr1: 247,530,709-247,571,796 , GRCh37.p13 chr1: 247,694,011-247,735,098 LOC102724446, GCSAML-AS1, 2 more genes
    nsv6668246copy number variation1nstd229human GRCh38 chr1: 247,205,066-247,563,960 , GRCh37.p13 chr1: 247,368,368-247,727,262 ZNF496, OR2B11, 13 more genes
    nsv6667957copy number variation1nstd229human GRCh38 chr1: 247,515,980-247,913,359 , GRCh37.p13 chr1: 247,679,282-248,076,661 OR2C3, OR6F1, 18 more genes
    nsv6666443copy number variation1nstd229human GRCh38 chr1: 247,360,102-247,648,912 , GRCh37.p13 chr1: 247,523,404-247,812,214 GCSAML-AS1, LOC102724446, 10 more genes
    nsv6659533copy number variation1nstd229human GRCh38 chr1: 247,373,080-248,325,181 , GRCh37.p13 chr1: 247,536,382-248,488,483 OR2L3, OR2L5, 47 more genes
    nsv6658452copy number variation1nstd229human GRCh38 chr1: 247,394,409-247,579,025 , GRCh37.p13 chr1: 247,557,711-247,742,327 LOC102724446, GCSAML-AS1, 5 more genes
    nsv6637119copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,671,905-247,981,897 , GRCh38.p12 chr1: 247,508,603-247,818,595 OR14K1, OR13G1, 13 more genes
    nsv6637024copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,588,318-248,022,379 , GRCh38.p12 chr1: 247,425,016-247,859,077 OR14L1, OR11L1, 20 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
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