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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961255insertion1nstd209human GRCh38 chr1: 200,127,697-200,127,697 , GRCh37.p13 chr1: 200,096,825-200,096,825 NR5A2
    nsv5886119copy number variation1nstd209human GRCh38 chr1: 200,113,188-200,113,237 , GRCh37.p13 chr1: 200,082,316-200,082,365 NR5A2
    nsv5883168copy number variation1nstd209human GRCh38 chr1: 200,094,777-200,095,723 , GRCh37.p13 chr1: 200,063,905-200,064,851 NR5A2
    nsv5878822copy number variation1nstd209human GRCh38 chr1: 200,094,737-200,095,756 , GRCh37.p13 chr1: 200,063,865-200,064,884 NR5A2
    nsv5877868copy number variation1nstd209human GRCh38 chr1: 200,165,006-200,165,140 , GRCh37.p13 chr1: 200,134,134-200,134,268 NR5A2
    nsv5730700mobile element insertion1nstd211human GRCh38 chr1: 200,112,223-200,112,223 , GRCh37.p13 chr1: 200,081,351-200,081,351 NR5A2
    nsv5680042mobile element insertion2nstd211human GRCh38 chr1: 200,142,981-200,142,981 , GRCh37.p13 chr1: 200,112,109-200,112,109 NR5A2
    nsv5679358mobile element insertion1nstd211human GRCh38 chr1: 200,081,825-200,081,825 , GRCh37.p13 chr1: 200,050,953-200,050,953 NR5A2
    nsv5620721insertion1nstd207human GRCh38 chr1: 200,107,812-200,107,812 , GRCh37.p13 chr1: 200,076,940-200,076,940 NR5A2, LOC107985244
    nsv5561392mobile element insertion1nstd206human GRCh38 chr1: 200,112,223-200,112,274 , GRCh37.p13 chr1: 200,081,351-200,081,402 NR5A2
    nsv5549573insertion1nstd206human GRCh38 chr1: 200,107,812-200,107,812 , GRCh37.p13 chr1: 200,076,940-200,076,940 NR5A2, LOC107985244
    nsv5452275copy number variation1nstd206human GRCh38 chr1: 200,094,687-200,095,659 , GRCh37.p13 chr1: 200,063,815-200,064,787 NR5A2
    nsv5449579copy number variation1nstd206human GRCh38 chr1: 200,155,893-200,170,066 , GRCh37.p13 chr1: 200,125,021-200,139,194 NR5A2
    nsv5448918copy number variation1nstd206human GRCh38 chr1: 200,117,678-200,117,980 , GRCh37.p13 chr1: 200,086,806-200,087,108 NR5A2
    nsv5448585copy number variation1nstd206human GRCh38 chr1: 200,052,446-200,052,772 , GRCh37.p13 chr1: 200,021,574-200,021,900 NR5A2, RNU6-570P
    nsv5442304copy number variation1nstd206human GRCh38 chr1: 200,013,291-200,025,710 , GRCh37.p13 chr1: 199,982,419-199,994,838 RNU6-609P, NR5A2
    nsv5440904copy number variation1nstd206human GRCh38 chr1: 200,052,415-200,052,509 , GRCh37.p13 chr1: 200,021,543-200,021,637 RNU6-570P, NR5A2
    nsv5400608mobile element insertion1nstd206human GRCh38 chr1: 200,081,825-200,081,876 , GRCh37.p13 chr1: 200,050,953-200,051,004 NR5A2
    nsv5396871mobile element insertion1nstd206human GRCh38 chr1: 200,142,981-200,143,032 , GRCh37.p13 chr1: 200,112,109-200,112,160 NR5A2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
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