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Items: 1 to 20 of 136

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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
    nsv6922411copy number variation1nstd229human GRCh38 chr12: 53,423,921-53,427,489 , GRCh37.p13 chr12: 53,817,705-53,821,273 AMHR2
    nsv6467064copy number variation1nstd223human GRCh38 chr12: 53,431,675-53,435,702 , GRCh37.p13 chr12: 53,825,459-53,829,486 AMHR2
    nsv6456879copy number variation1nstd223human GRCh38 chr12: 53,423,701-53,425,900 , GRCh37.p13 chr12: 53,817,485-53,819,684 AMHR2
    nsv6241042mobile element insertion1nstd215human GRCh38 chr12: 53,428,202-53,428,202 , GRCh37.p13 chr12: 53,821,986-53,821,986 AMHR2
    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
    nsv6094236insertion1nstd212human GRCh38 chr12: 53,428,191-53,428,191 , GRCh37.p13 chr12: 53,821,975-53,821,975 AMHR2
    nsv5708170mobile element insertion2nstd211human GRCh38 chr12: 53,428,202-53,428,202 , GRCh37.p13 chr12: 53,821,986-53,821,986 AMHR2
    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
    nsv5131773mobile element insertion1nstd203human GRCh38 chr12: 53,428,191-53,428,202 , GRCh37.p13 chr12: 53,821,975-53,821,986 AMHR2
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4835886copy number variation1nstd200human GRCh37 chr12: 53,814,882-53,816,819 , GRCh38.p12 chr12: 53,421,098-53,423,035 AMHR2
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4729204copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 53,614,278-53,971,802 , GRCh38.p12 chr12: 53,220,494-53,578,018 AMHR2, PCBP2, 18 more genes
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