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Items: 1 to 20 of 2990

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148242copy number variation1nstd102humanPathogenic GRCh38 chr15: 20,966,971-25,963,714 , GRCh37.p13 chr15: 21,172,300-26,208,861 LOC101269108, LOC107983983, 227 more genes
    nsv7148205copy number variation1nstd102humanPathogenic GRCh38 chr15: 25,354,042-25,357,067 , GRCh37.p13 chr15: 25,599,189-25,602,214 SNHG14, UBE3A
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7148097copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,605,427-28,566,579 , GRCh38.p12 chr15: 23,360,280-28,321,433 LOC107984770, SNORD115-31, 147 more genes
    nsv7147536insertion1nstd232human GRCh37.p13 chr15: 25,137,670-25,137,670 , GRCh38.p12 chr15: 24,892,523-24,892,523 SNRPN, SNHG14
    nsv7140732copy number variation1nstd232human GRCh37.p13 chr15: 25,126,673-25,126,731 , GRCh38.p12 chr15: 24,881,526-24,881,584 SNRPN, SNHG14
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7137100copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,691-28,566,579 , GRCh38.p12 chr15: 23,439,544-28,321,433 DMAC1P1, SNORD116-16, 142 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7098730copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 22,833,523-25,223,593 , GRCh38.p12 chr15: 23,319,714-24,978,446 NDN, SNRPN, 30 more genes
    nsv7094357copy number variation1nstd102humanPathogenic GRCh37 chr15: 25,615,693-25,650,609 , GRCh38.p12 chr15: 25,370,546-25,405,462 SNHG14, UBE3A
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7093400copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,645-28,566,612 , GRCh38.p12 chr15: 23,439,498-28,321,466 SNORD115-45, SNORD107, 142 more genes
    nsv7093227copy number variation1nstd102humanPathogenic GRCh37 chr15: 25,197,764-25,207,033 , GRCh38 chr15: 24,952,617-24,961,886 SNRPN, SNURF, 1 more genes
    nsv7076002inversion1nstd229human GRCh38 chr15: 24,690,749-24,837,056 , GRCh37.p13 chr15: 24,935,896-25,082,203 SNRPN, SNHG14
    nsv7075691inversion1nstd229human GRCh38 chr15: 24,928,808-24,931,630 , GRCh37.p13 chr15: 25,173,955-25,176,777 SNRPN, SNHG14
    nsv7075342inversion1nstd229human GRCh38 chr15: 24,919,026-25,051,406 , GRCh37.p13 chr15: 25,164,173-25,296,553 SNORD64, PWARSN, 9 more genes
    nsv7072258inversion1nstd229human GRCh38 chr15: 24,964,778-24,964,858 , GRCh37.p13 chr15: 25,209,925-25,210,005 SNRPN, SNURF, 1 more genes
    nsv7072235inversion1nstd229human GRCh38 chr15: 23,679,022-24,873,610 , GRCh37.p13 chr15: 23,924,169-25,118,757 PWRN2, LOC107984787, 12 more genes
    nsv7070071inversion1nstd229human GRCh38 chr15: 25,391,027-25,602,151 , GRCh37.p13 chr15: 25,636,174-25,847,298 UBE3A, SNHG14, 2 more genes
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