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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5687595mobile element insertion1nstd211human GRCh38 chr1: 221,707,818-221,707,818 , GRCh37.p13 chr1: 221,881,160-221,881,160 , DUSP10
    nsv5538095insertion1nstd206human GRCh38 chr1: 221,707,818-221,707,850 , GRCh37.p13 chr1: 221,881,160-221,881,192 , DUSP10
    nsv5537879insertion1nstd206human GRCh38 chr1: 221,700,580-221,700,620 , GRCh37.p13 chr1: 221,873,922-221,873,962 DUSP10
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5071934mobile element insertion1nstd203human GRCh38 chr1: 221,726,668-221,726,674 , GRCh37.p13 chr1: 221,900,010-221,900,016 DUSP10
    nsv4898868copy number variation1nstd200human GRCh38 chr1: 221,570,183-221,762,525 , GRCh37.p13 chr1: 221,743,525-221,935,867 , DUSP10, 1 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 HLX-AS1, OPN3, 740 more genes
    nsv4674785copy number variation1nstd102humanPathogenic GRCh37 chr1: 219,916,966-239,004,378 , GRCh38.p12 chr1: 219,743,624-238,841,078 RPL23AP23, LOC101927143, 414 more genes
    nsv4674721copy number variation1nstd102humanPathogenic GRCh37 chr1: 219,734,913-224,104,993 , GRCh38.p12 chr1: 219,561,571-223,917,291 PRELID3BP1, RNU6-403P, 82 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 RNA5S8, NTPCR, 893 more genes
    nsv4533542insertion1nstd166human GRCh37.p13 chr1: 221,873,911-221,873,911 , GRCh38.p12 chr1: 221,700,569-221,700,569 DUSP10
    nsv4460339mobile element insertion1nstd166human GRCh37.p13 chr1: 221,909,235-221,909,235 , GRCh38.p12 chr1: 221,735,893-221,735,893 DUSP10
    nsv4452084copy number variation1nstd102humanUncertain significance GRCh37 chr1: 219,379,258-222,049,547 , GRCh38.p12 chr1: 219,205,916-221,876,205 RNU6-403P, RPS15AP12, 46 more genes
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 RGS18, LINC02257, 1186 more genes
    nsv4071456copy number variation1nstd166human GRCh37.p13 chr1: 221,880,820-221,884,538 , GRCh38.p12 chr1: 221,707,478-221,711,196 , DUSP10
    nsv4058174copy number variation1nstd166human GRCh37.p13 chr1: 221,901,711-221,909,319 , GRCh38.p12 chr1: 221,728,369-221,735,977 DUSP10
    nsv3964435copy number variation1nstd168human GRCh38 chr1: 221,630,419-221,742,473 , GRCh37.p13 chr1: 221,803,761-221,915,815 , DUSP10
    nsv3921757copy number variation1nstd102humannot provided NCBI36 chr1: 214,401,568-247,249,719 , GRCh37.p13 chr1: 216,334,945-249,233,096 , GRCh38.p12 chr1: 216,161,603-248,938,897 MTCYBP15, RNU4-77P, 658 more genes
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