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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681662copy number variation1nstd102humanPathogenic GRCh37 chr10: 72,357,789-72,360,678 , GRCh38.p12 chr10: 70,598,033-70,600,922 PRF1
    nsv7093726copy number variation1nstd102humanUncertain significance GRCh37 chr10: 72,357,809-72,360,658 , GRCh38.p12 chr10: 70,598,053-70,600,902 PRF1
    nsv5380872copy number variation2nstd102humanUncertain significance GRCh37 chr10: 72,179,670-72,360,658 , GRCh38.p12 chr10: 70,419,914-70,600,902 PRF1, NODAL, 3 more genes
    nsv3895731copy number variation1nstd102humanUncertain significance GRCh37 chr8: 28,236,568-28,385,305 , GRCh38.p12 chr8: 28,379,051-28,527,788 ZNF395, RNU6-178P, 3 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 PRF1, RNU7-12P, 1876 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv3916527copy number variation1nstd102humanPathogenic NCBI36 chr8: 15,137,722-32,366,274 , GRCh37.p13 chr8: 15,093,351-32,246,732 , GRCh38.p12 chr8: 15,235,842-32,389,216 LOC105379343, INTS10, 281 more genes
    nsv3921296copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,383,584-29,033,946 , NCBI36 chr8: 12,285,464-28,947,382 , GRCh37 chr8: 12,241,093-28,891,463 XPO7, ADRA1A, 264 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 PRF1, UNC5B-AS1, 250 more genes
    nsv3923174copy number variation1nstd102humanPathogenic GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324 RPLP1P9, CHRNA2, 259 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 PRF1, MYL6P3, 220 more genes
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 PRF1, SLC25A16, 204 more genes
    nsv3919731copy number variation1nstd102humanPathogenic GRCh38 chr8: 25,171,103-31,750,600 , NCBI36 chr8: 25,084,535-31,727,658 , GRCh37 chr8: 25,028,618-31,608,116 LOC100131127, MIR4287, 122 more genes
    nsv3923302copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253 BNIP3L, RNU6-178P, 123 more genes
    nsv3911687copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,196,357 , NCBI36 chr8: 24,823,781-31,173,415 , GRCh37 chr8: 24,767,877-31,053,873 EXTL3-AS1, RNA5SP258, 123 more genes
    nsv4675292copy number variation1nstd102humanPathogenic GRCh37 chr8: 24,305,969-28,673,405 , GRCh38.p12 chr8: 24,448,456-28,815,888 LOC112268023, GNRH1, 79 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 RN7SL474P, UNC5D, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 TBC1D31, LOC105375740, 2109 more genes
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