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Items: 1 to 20 of 350

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977099inversion1nstd209human GRCh38 chr10: 50,024,649-50,153,348 , GRCh37.p13 chr10|NW_004504302.1: 203,824-305,900 SLC9A3P1, WASHC2A, 2 more genes
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5865810copy number variation1nstd209human GRCh38 chr10: 50,108,823-50,111,690 , GRCh37.p13 chr10|NW_004504302.1: 287,998-290,865 WASHC2A
    nsv5857685copy number variation1nstd209human GRCh38 chr10: 50,065,332-50,067,831 , GRCh37.p13 chr10|NW_004504302.1: 244,507-247,006 , GRCh37.p13 chr10: 51,825,092-51,827,591 WASHC2A, FAM21EP
    nsv5850005copy number variation1nstd209human GRCh38 chr10: 50,065,669-50,067,609 , GRCh37.p13 chr10|NW_004504302.1: 244,844-246,784 , GRCh37.p13 chr10: 51,825,429-51,827,369 FAM21EP, WASHC2A
    nsv5847915copy number variation1nstd209human GRCh38 chr10: 50,120,195-50,122,254 , GRCh37.p13 chr10|NW_004504302.1: 299,370-301,429 WASHC2A
    nsv5718567mobile element insertion1nstd211human GRCh38 chr10: 50,094,993-50,094,993 , GRCh37.p13 chr10|NW_004504302.1: 274,168-274,168 WASHC2A
    nsv5627640insertion1nstd207human GRCh38 chr10: 50,066,625-50,066,625 , GRCh37.p13 chr10|NW_004504302.1: 245,800-245,800 , GRCh37.p13 chr10: 51,826,385-51,826,385 WASHC2A, FAM21EP
    nsv5625986insertion1nstd207human GRCh38 chr10: 50,097,286-50,097,286 , GRCh37.p13 chr10|NW_004504302.1: 276,461-276,461 WASHC2A
    nsv5624957insertion1nstd207human GRCh38 chr10: 50,124,869-50,124,869 , GRCh37.p13 chr10|NW_004504302.1: 304,044-304,044 WASHC2A
    nsv5624544insertion1nstd207human GRCh38 chr10: 50,076,816-50,076,816 , GRCh37.p13 chr10|NW_004504302.1: 255,991-255,991 WASHC2A
    nsv5562022sequence alteration1nstd206human GRCh37.p13 chr10|NW_004504302.1: 231,304-281,503 , GRCh38 chr10: 50,052,129-50,102,328 WASHC2A, FAM21EP
    nsv5561160inversion1nstd206human GRCh37.p13 chr10|NW_004504302.1: 231,161-281,725 , GRCh38 chr10: 50,051,986-50,102,550 WASHC2A, FAM21EP
    nsv5558882sequence alteration1nstd206human GRCh37.p13 chr10|NW_004504302.1: 222,798-305,900 , GRCh38 chr10: 50,043,623-50,135,706 , GRCh37.p13 chr10: 47,892,478-47,946,220 WASHC2A, FAM21EP
    nsv5493106copy number variation1nstd206human GRCh38 chr10: 50,086,368-50,112,368 , GRCh37.p13 chr10|NW_004504302.1: 265,543-291,543 WASHC2A
    nsv5484680copy number variation1nstd206human GRCh38 chr10: 50,076,707-50,076,882 , GRCh37.p13 chr10|NW_004504302.1: 255,882-256,057 WASHC2A
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5478460copy number variation1nstd206human GRCh37.p13 chr10|NW_004504302.1: 177,409-250,675 , GRCh38 chr10: 49,998,234-50,071,500 , GRCh37.p13 chr10: 51,757,994-51,831,260 AGAP6, WASHC2A, 3 more genes
    nsv5259975copy number variation1nstd204human GRCh38.p13 chr10: 50,132,475-50,135,002 , GRCh37.p13 chr10: 51,892,235-51,894,762 WASHC2A
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