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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6689723copy number variation1nstd229human GRCh38 chr2: 176,082,201-176,178,200 , GRCh37.p13 chr2: 176,946,929-177,042,928 HOXD9, HOXD12, 13 more genes
    nsv6687608copy number variation1nstd229human GRCh38 chr2: 176,115,628-176,121,503 , GRCh37.p13 chr2: 176,980,356-176,986,231 HOXD10, HOXD9
    nsv6637115copy number variation1nstd102humanPathogenic GRCh37 chr2: 175,143,352-180,999,636 , GRCh38.p12 chr2: 174,278,624-180,134,909 RNU6-5P, LOC101927073, 107 more genes
    nsv6636209copy number variation1nstd102humanUncertain significance GRCh37 chr2: 176,988,535-177,046,403 , GRCh38.p12 chr2: 176,123,807-176,181,675 HAGLR, LOC100129455, 8 more genes
    nsv6627785copy number variation1nstd224human GRCh37 chr2: 176,957,878-177,036,574 , GRCh38.p12 chr2: 176,093,150-176,171,846 HOXD8, HOXD11, 11 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315016copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,524,396-178,694,337 , GRCh38.p12 chr2: 170,667,886-177,829,610 LOC105373746, HAGLROS, 136 more genes
    nsv6291326copy number variation1nstd102humannot provided GRCh37 chr2: 174,631,045-177,365,790 , GRCh38.p12 chr2: 173,766,317-176,501,062 RNU6-5P, RPS15AP14, 56 more genes
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 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
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
    nsv5216071copy number variation1nstd204human GRCh38.p13 chr2: 176,118,589-176,121,507 , GRCh37.p13 chr2: 176,983,317-176,986,235 HOXD10, HOXD9
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv4674757copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858 OSBPL6, DNAJC19P5, 256 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4454648copy number variation1nstd102humanPathogenic GRCh37 chr2: 173,538,954-186,401,606 , GRCh38.p12 chr2: 172,674,226-185,536,879 PDE11A, LOC100289479, 176 more genes
    nsv4452748copy number variation1nstd102humanPathogenic GRCh37 chr2: 176,310,551-179,092,634 , GRCh38.p12 chr2: 175,445,823-178,227,907 LOC105373760, LOC105369143, 63 more genes
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