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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
    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
    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
    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
    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
    nsv7062202inversion1nstd229human GRCh38 chr15: 24,015,385-25,754,615 , GRCh37.p13 chr15: 24,260,532-25,999,762 ATP10A, SNORD115-4, 107 more genes
    nsv7060175inversion1nstd229human GRCh38 chr15: 23,786,777-25,729,649 , GRCh37.p13 chr15: 24,031,924-25,974,796 SNORD115-26, LOC107984787, 107 more genes
    nsv6973165copy number variation1nstd229human GRCh38 chr15: 23,199,056-28,429,484 , GRCh37.p13 chr15: 23,564,855-28,674,630 LOC102723564, SNORD115-2, 162 more genes
    nsv6971742copy number variation1nstd229human GRCh38 chr15: 25,185,301-25,320,500 , GRCh37.p13 chr15: 25,430,448-25,565,647 SNORD115-40, SNORD115-43, 41 more genes
    nsv6969131copy number variation1nstd229human GRCh38 chr15: 22,744,959-28,819,371 , GRCh37.p13 chr15: 23,564,855-29,064,517 RNA5SP391, PDCD6IPP1, 195 more genes
    nsv6968122copy number variation1nstd229human GRCh38 chr15: 25,247,681-25,251,186 , GRCh37.p13 chr15: 25,492,828-25,496,333 SNORD115-44, SNHG14, 2 more genes
    nsv6967195copy number variation1nstd229human GRCh38 chr15: 25,229,941-25,253,866 , GRCh37.p13 chr15: 25,475,088-25,499,013 SNORD115-34, SNORD115-42, 11 more genes
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
    nsv6637553copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-30,386,553 , GRCh38.p12 chr15: 23,319,714-30,094,350 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, LOC105370751, 247 more genes
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