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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7042448inversion1nstd229human GRCh38 chr1: 37,963,756-37,964,977 , GRCh37.p13 chr1: 38,429,428-38,430,649 SF3A3
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649607copy number variation1nstd229human GRCh38 chr1: 37,972,946-37,975,923 , GRCh37.p13 chr1: 38,438,618-38,441,595 SF3A3
    nsv6649606copy number variation1nstd229human GRCh38 chr1: 37,952,501-37,957,400 , GRCh37.p13 chr1: 38,418,173-38,423,072 SF3A3
    nsv6649572copy number variation1nstd229human GRCh38 chr1: 37,745,813-38,046,235 , GRCh37.p13 chr1: 38,211,485-38,511,907 C1orf122, RPS2P13, 15 more genes
    nsv6649517copy number variation1nstd229human GRCh38 chr1: 37,933,618-37,984,899 , GRCh37.p13 chr1: 38,399,290-38,450,571 LOC105378651, SF3A3, 1 more genes
    nsv6649083copy number variation1nstd229human GRCh38 chr1: 37,960,601-37,964,700 , GRCh37.p13 chr1: 38,426,273-38,430,372 SF3A3
    nsv6649082copy number variation1nstd229human GRCh38 chr1: 37,955,290-37,961,825 , GRCh37.p13 chr1: 38,420,962-38,427,497 SF3A3
    nsv6649078copy number variation1nstd229human GRCh38 chr1: 37,894,301-38,107,800 , GRCh37.p13 chr1: 38,359,973-38,573,472 MIR3659, FHL3, 7 more genes
    nsv6546968inversion1nstd223human GRCh38 chr1: 37,980,241-37,980,964 , GRCh37.p13 chr1: 38,445,913-38,446,636 SF3A3
    nsv6535831inversion1nstd223human GRCh38 chr1: 37,986,122-37,986,752 , GRCh37.p13 chr1: 38,451,794-38,452,424 SF3A3
    nsv6326159copy number variation1nstd223human GRCh38 chr1: 37,963,926-37,966,994 , GRCh37.p13 chr1: 38,429,598-38,432,666 SF3A3
    nsv6319747copy number variation1nstd223human GRCh38 chr1: 37,970,028-37,971,436 , GRCh37.p13 chr1: 38,435,700-38,437,108 SF3A3
    nsv6316644copy number variation1nstd223human GRCh38 chr1: 37,964,433-37,966,029 , GRCh37.p13 chr1: 38,430,105-38,431,701 SF3A3
    nsv6315661copy number variation1nstd223human GRCh38 chr1: 37,963,954-37,964,888 , GRCh37.p13 chr1: 38,429,626-38,430,560 SF3A3
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6251583mobile element insertion1nstd215human GRCh38 chr1: 37,982,045-37,982,045 , GRCh37.p13 chr1: 38,447,717-38,447,717 SF3A3
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