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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095762copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,435,087-169,455,004 , GRCh38.p12 chr1: 169,465,849-169,485,766 SLC19A2
    nsv7095711copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,454,781-169,455,004 , GRCh38.p12 chr1: 169,485,543-169,485,766 SLC19A2
    nsv6644471copy number variation1nstd229human GRCh38 chr1: 169,473,801-169,475,100 , GRCh37.p13 chr1: 169,443,039-169,444,338 SLC19A2
    nsv6644402copy number variation1nstd229human GRCh38 chr1: 169,471,458-169,478,141 , GRCh37.p13 chr1: 169,440,696-169,447,379 SLC19A2
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644032copy number variation1nstd229human GRCh38 chr1: 169,479,868-169,501,061 , GRCh37.p13 chr1: 169,449,106-169,470,299 SLC19A2
    nsv6331577copy number variation1nstd223human GRCh38 chr1: 169,481,801-169,487,700 , GRCh37.p13 chr1: 169,451,039-169,456,938 SLC19A2
    nsv6330515copy number variation1nstd223human GRCh38 chr1: 169,470,311-169,471,848 , GRCh37.p13 chr1: 169,439,549-169,441,086 SLC19A2
    nsv6327166copy number variation1nstd223human GRCh38 chr1: 169,466,408-169,466,725 , GRCh37.p13 chr1: 169,435,646-169,435,963 SLC19A2
    nsv6319131copy number variation1nstd223human GRCh38 chr1: 169,473,802-169,474,991 , GRCh37.p13 chr1: 169,443,040-169,444,229 SLC19A2
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6245581mobile element insertion1nstd215human GRCh38 chr1: 169,473,736-169,473,736 , GRCh37.p13 chr1: 169,442,974-169,442,974 SLC19A2
    nsv6133937copy number variation1nstd213human GRCh37 chr1: 167,800,000-169,660,001 , GRCh38.p12 chr1: 167,830,762-169,690,860 XCL2, TBX19, 38 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133597copy number variation1nstd213human GRCh37 chr1: 167,470,000-170,370,001 , GRCh38.p12 chr1: 167,500,763-170,400,860 CD247, XCL1, 64 more genes
    nsv6133565copy number variation1nstd213human GRCh37 chr1: 164,310,000-170,640,001 , GRCh38.p12 chr1: 164,340,763-170,670,860 ATP1B1, DPT, 126 more genes
    nsv6052125insertion1nstd212human GRCh38 chr1: 169,482,243-169,482,243 , GRCh37.p13 chr1: 169,451,481-169,451,481 SLC19A2
    nsv6051538insertion1nstd212human GRCh38 chr1: 169,473,717-169,473,717 , GRCh37.p13 chr1: 169,442,955-169,442,955 SLC19A2
    nsv5981939copy number variation1nstd212human GRCh38 chr1: 169,474,885-169,475,056 , GRCh37.p13 chr1: 169,444,123-169,444,294 SLC19A2
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