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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099223copy number variation1nstd231human GRCh38.p12 chr1: 108,551,579-110,710,631 , GRCh37 chr1: 109,094,201-111,253,253 ALX3, AMPD2, 74 more genes
    nsv7095739copy number variation1nstd102humanPathogenic GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554 RPL7L1P21, GSTM4, 90 more genes
    nsv6639759copy number variation1nstd229human GRCh38 chr1: 109,621,602-109,627,282 , GRCh37.p13 chr1: 110,164,224-110,169,904 AMPD2
    nsv6639673copy number variation1nstd229human GRCh38 chr1: 109,619,695-109,619,737 , GRCh37.p13 chr1: 110,162,317-110,162,359 GNAT2, AMPD2
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6310515copy number variation1nstd102humanUncertain significance GRCh37 chr1: 110,145,976-110,173,774 , GRCh38.p12 chr1: 109,603,354-109,631,152 GNAT2, AMPD2
    nsv6290678copy number variation1nstd102humanUncertain significance GRCh37 chr1: 108,346,477-110,177,123 , GRCh38.p12 chr1: 107,803,855-109,634,501 SYPL2, NDUFB3P1, 53 more genes
    nsv6133726copy number variation1nstd213human GRCh37 chr1: 109,950,000-110,240,001 , GRCh38.p12 chr1: 109,407,378-109,697,379 AMPD2, GNAI3, 14 more genes
    nsv5431073copy number variation1nstd206human GRCh38 chr1: 109,590,493-109,903,664 , GRCh37.p13 chr1: 110,133,115-110,446,286 GSTM3, GSTM1, 12 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5293062copy number variation1nstd204human GRCh38.p13 chr1: 109,590,471-109,903,689 , GRCh37.p13 chr1: 110,133,093-110,446,311 RNU6V, GSTM2, 12 more genes
    nsv5215481copy number variation1nstd204human GRCh38.p13 chr1: 109,590,501-109,644,400 , GRCh37.p13 chr1: 110,133,123-110,187,022 GNAI3, RNU6V, 3 more genes
    nsv5213581copy number variation1nstd204human GRCh38.p13 chr1: 109,618,275-109,644,467 , GRCh37.p13 chr1: 110,160,897-110,187,089 AMPD2, GNAT2
    nsv4781111copy number variation1nstd200human GRCh37 chr1: 110,133,115-110,446,286 , GRCh38.p12 chr1: 109,590,493-109,903,664 AMPD2, MIR197, 12 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4453642copy number variation1nstd102humannot provided GRCh37 chr1: 108,926,313-111,266,497 , GRCh38.p12 chr1: 108,383,691-110,723,875 PSMA5, GSTM1, 79 more genes
    nsv4436700copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 107,779,092-111,199,205 , GRCh38.p12 chr1: 107,236,470-110,656,583 ALX3, AMPD2, 89 more genes
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