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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv7137008copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,443,916-28,451,385 , GRCh38.p12 chr15: 28,198,770-28,206,239 , GRCh38.p12 chr15|NW_011332701.1: 332,211-339,707 HERC2
    nsv7136957copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,538,169-28,566,507 , GRCh38.p12 chr15: 28,293,023-28,321,361 , GRCh38.p12 chr15|NT_187660.1: 540,248-568,585 , GRCh38.p12 chr15|NW_011332701.1: 426,462-454,799 HERC2, RPL41P2
    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
    nsv7094526copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,544,548-28,544,662 , GRCh38.p12 chr15: 28,299,402-28,299,516 , GRCh38.p12 chr15|NT_187660.1: 546,626-546,740 , GRCh38.p12 chr15|NW_011332701.1: 432,840-432,954 HERC2
    nsv7094464copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,475,513-28,475,646 , GRCh38.p12 chr15: 28,230,367-28,230,500 , GRCh38.p12 chr15|NW_011332701.1: 363,829-363,962 HERC2
    nsv7094362copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,267,627-28,391,510 , GRCh38.p12 chr15: 28,022,481-28,146,364 , GRCh38.p12 chr15|NT_187660.1: 156,780-279,806 , GRCh38.p12 chr15|NW_011332701.1: 156,780-279,806 OCA2, HERC2
    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
    nsv7075933inversion1nstd229human GRCh38 chr15: 27,763,634-29,945,003 , GRCh37.p13 chr15: 28,008,780-30,237,206 RN7SL719P, ENTREP2, 39 more genes
    nsv7074171inversion1nstd229human GRCh38 chr15: 27,576,188-29,433,618 , GRCh37.p13 chr15: 27,821,334-29,725,822 MPHOSPH10P7, RN7SL238P, 34 more genes
    nsv7071113inversion1nstd229human GRCh38 chr15: 27,800,030-28,154,445 , GRCh37.p13 chr15: 28,045,176-28,399,591 RPL5P32, OCA2, 1 more genes
    nsv7069807inversion1nstd229human GRCh38 chr15: 28,247,887-28,655,501 , GRCh37.p13 chr15: 28,493,033-28,900,647 LOC101059997, MIR4509-2, 17 more genes
    nsv7067542inversion1nstd229human GRCh38 chr15: 23,549,781-28,456,830 , GRCh37.p13 chr15: 23,794,928-28,701,976 SNORD115-34, LOC107984787, 148 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv7065294inversion1nstd229human GRCh38 chr15: 27,010,857-29,330,650 , GRCh37.p13 chr15: 27,256,004-29,622,854 GABRG3-AS1, HERC2P1, 40 more genes
    nsv6976252copy number variation1nstd229human GRCh38 chr15: 28,032,233-28,164,477 , GRCh37.p13 chr15: 28,277,379-28,409,623 HERC2, OCA2
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