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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv6936585copy number variation1nstd229human GRCh38 chr12: 53,384,414-53,387,941 , GRCh37.p13 chr12: 53,778,198-53,781,725 SP1
    nsv6930486copy number variation1nstd229human GRCh38 chr12: 53,391,322-53,391,361 , GRCh37.p13 chr12: 53,785,106-53,785,145 SP1
    nsv6927865copy number variation1nstd229human GRCh38 chr12: 53,397,963-53,402,062 , GRCh37.p13 chr12: 53,791,747-53,795,846 SP1
    nsv6594140inversion1nstd223human GRCh38 chr12: 53,393,620-53,394,099 , GRCh37.p13 chr12: 53,787,404-53,787,883 SP1
    nsv6580222inversion1nstd223human GRCh38 chr12: 53,395,952-53,397,481 , GRCh37.p13 chr12: 53,789,736-53,791,265 SP1
    nsv6468750copy number variation1nstd223human GRCh38 chr12: 53,384,254-53,392,568 , GRCh37.p13 chr12: 53,778,038-53,786,352 SP1
    nsv6466304copy number variation1nstd223human GRCh38 chr12: 53,391,597-53,393,878 , GRCh37.p13 chr12: 53,785,381-53,787,662 SP1
    nsv6461442copy number variation1nstd223human GRCh38 chr12: 53,378,053-53,378,927 , GRCh37.p13 chr12: 53,771,837-53,772,711 SP1
    nsv6458608copy number variation1nstd223human GRCh38 chr12: 53,389,701-53,392,400 , GRCh37.p13 chr12: 53,783,485-53,786,184 SP1
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132426copy number variation1nstd213human GRCh37 chr12: 52,740,000-55,260,001 , GRCh38.p12 chr12: 52,346,216-54,866,217 , HOXC4, 122 more genes
    nsv5946119copy number variation1nstd209human GRCh38 chr12: 53,409,964-53,410,258 , GRCh37.p13 chr12: 53,803,748-53,804,042 SP1
    nsv5942842copy number variation1nstd209human GRCh38 chr12: 53,399,596-53,402,486 , GRCh37.p13 chr12: 53,793,380-53,796,270 SP1
    nsv5928761copy number variation1nstd209human GRCh38 chr12: 53,378,053-53,378,926 , GRCh37.p13 chr12: 53,771,837-53,772,710 SP1
    nsv5509214copy number variation1nstd206human GRCh38 chr12: 53,378,055-53,378,927 , GRCh37.p13 chr12: 53,771,839-53,772,711 SP1
    nsv5269754copy number variation1nstd204human GRCh38.p13 chr12: 53,319,601-53,446,000 , GRCh37.p13 chr12: 53,713,385-53,839,784 SP7, PRR13, 3 more genes
    nsv5266008copy number variation1nstd204human GRCh38.p13 chr12: 53,248,501-53,495,800 , GRCh37.p13 chr12: 53,642,285-53,889,584 PCBP2, AAAS, 11 more genes
    nsv5196162mobile element insertion1nstd203human GRCh38 chr12: 53,416,784-53,416,784 , GRCh37.p13 chr12: 53,810,568-53,810,568 SP1
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