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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139505insertion1nstd232human GRCh37.p13 chr1: 55,611,783-55,611,783 , GRCh38.p12 chr1: 55,146,110-55,146,110 USP24
    nsv7099206copy number variation1nstd231human GRCh38.p12 chr1: 54,693,460-58,571,894 , GRCh37 chr1: 55,159,133-59,037,566 C8A, C8B, 49 more genes
    nsv7053230inversion1nstd229human GRCh38 chr1: 54,133,615-56,561,151 , GRCh37.p13 chr1: 54,599,288-57,026,824 GOT2P1, CIMAP2, 41 more genes
    nsv7040702inversion1nstd229human GRCh38 chr1: 55,164,138-55,164,179 , GRCh37.p13 chr1: 55,629,811-55,629,852 USP24
    nsv6652208copy number variation1nstd229human GRCh38 chr1: 55,215,573-55,220,327 , GRCh37.p13 chr1: 55,681,246-55,686,000 USP24, GYG1P3, 2 more genes
    nsv6652000copy number variation1nstd229human GRCh38 chr1: 55,203,833-55,203,913 , GRCh37.p13 chr1: 55,669,506-55,669,586 USP24
    nsv6651980copy number variation1nstd229human GRCh38 chr1: 55,079,757-55,079,815 , GRCh37.p13 chr1: 55,545,430-55,545,488 USP24
    nsv6651895copy number variation1nstd229human GRCh38 chr1: 55,189,704-55,193,048 , GRCh37.p13 chr1: 55,655,377-55,658,721 USP24
    nsv6651893copy number variation1nstd229human GRCh38 chr1: 55,032,508-55,066,132 , GRCh37.p13 chr1: 55,498,181-55,531,805 USP24, PCSK9
    nsv6651884copy number variation1nstd229human GRCh38 chr1: 54,798,403-55,085,262 , GRCh37.p13 chr1: 55,264,076-55,550,935 PCSK9, TTC22, 8 more genes
    nsv6554665inversion1nstd223human GRCh38 chr1: 55,107,831-55,109,168 , GRCh37.p13 chr1: 55,573,504-55,574,841 USP24
    nsv6539047inversion1nstd223human GRCh38 chr1: 55,201,635-55,202,356 , GRCh37.p13 chr1: 55,667,308-55,668,029 USP24
    nsv6333365copy number variation1nstd223human GRCh38 chr1: 55,167,694-55,168,066 , GRCh37.p13 chr1: 55,633,367-55,633,739 USP24
    nsv6327503copy number variation1nstd223human GRCh38 chr1: 55,170,078-55,170,473 , GRCh37.p13 chr1: 55,635,751-55,636,146 USP24
    nsv6322181copy number variation1nstd223human GRCh38 chr1: 55,154,743-55,155,225 , GRCh37.p13 chr1: 55,620,416-55,620,898 USP24
    nsv6321115copy number variation1nstd223human GRCh38 chr1: 55,120,137-55,120,537 , GRCh37.p13 chr1: 55,585,810-55,586,210 USP24
    nsv6319283copy number variation1nstd223human GRCh38 chr1: 55,156,301-55,157,300 , GRCh37.p13 chr1: 55,621,974-55,622,973 USP24
    nsv6318669copy number variation1nstd223human GRCh38 chr1: 55,145,401-55,146,700 , GRCh37.p13 chr1: 55,611,074-55,612,373 USP24
    nsv6317636copy number variation1nstd223human GRCh38 chr1: 55,211,501-55,214,800 , GRCh37.p13 chr1: 55,677,174-55,680,473 LOC100507634, USP24
    nsv6316473copy number variation1nstd223human GRCh38 chr1: 55,215,573-55,220,324 , GRCh37.p13 chr1: 55,681,246-55,685,997 MIR4422HG, LOC100507634, 2 more genes
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