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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962993insertion1nstd209human GRCh38 chr6: 112,241,152-112,241,152 , GRCh37.p13 chr6|NW_003871062.1: 238,673-238,673 , GRCh37.p13 chr6: 112,562,353-112,562,353 LAMA4-AS1, LAMA4
    nsv5686603mobile element insertion1nstd211human GRCh38 chr6: 112,260,387-112,260,387 , GRCh37.p13 chr6: 112,581,589-112,581,589 , GRCh37.p13 chr6|NW_003871062.1: 257,908-257,908 LAMA4-AS1
    nsv5639355insertion1nstd207human GRCh38 chr6: 112,241,152-112,241,152 , GRCh37.p13 chr6|NW_003871062.1: 238,673-238,673 , GRCh37.p13 chr6: 112,562,353-112,562,353 LAMA4-AS1, LAMA4
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5461572copy number variation1nstd206human GRCh38 chr6: 112,296,696-112,300,742 , GRCh37.p13 chr6: 112,617,898-112,621,944 LAMA4-AS1, LOC107986632
    nsv5116399mobile element insertion1nstd203human GRCh38 chr6: 112,236,461-112,236,470 , GRCh37.p13 chr6|NW_003871062.1: 233,982-233,991 , GRCh37.p13 chr6: 112,557,662-112,557,671 LAMA4-AS1, LAMA4
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4948209copy number variation1nstd200human GRCh38 chr6: 112,296,696-112,300,742 , GRCh37.p13 chr6: 112,617,898-112,621,944 LAMA4-AS1, LOC107986632
    nsv4948208copy number variation1nstd200human GRCh38 chr6: 112,254,343-112,255,390 , GRCh37.p13 chr6|NW_003871062.1: 251,864-252,911 , GRCh37.p13 chr6: 112,575,545-112,576,592 LAMA4, LAMA4-AS1
    nsv4945569copy number variation1nstd200human GRCh38 chr6: 112,291,456-113,231,784 , GRCh37.p13 chr6: 112,612,658-113,552,986 , RNU6-1163P, 20 more genes
    nsv4945568copy number variation1nstd200human GRCh38 chr6: 112,282,798-112,403,117 , GRCh37.p13 chr6: 112,604,000-112,724,319 RPSAP45, RFPL4B, 6 more genes
    nsv4945567copy number variation1nstd200human GRCh38 chr6: 112,248,448-112,262,077 , GRCh37.p13 chr6: 112,569,650-112,583,279 , GRCh37.p13 chr6|NW_003871062.1: 245,969-259,598 LAMA4, LAMA4-AS1
    nsv4824633copy number variation1nstd200human GRCh37 chr6: 112,569,650-112,583,278 , GRCh38.p12 chr6: 112,248,448-112,262,076 LAMA4, LAMA4-AS1
    nsv4817560copy number variation1nstd200human GRCh37 chr6: 112,617,898-112,621,944 , GRCh38.p12 chr6: 112,296,696-112,300,742 LAMA4-AS1, LOC107986632
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4763856insertion1nstd199human GRCh37 chr6: 112,562,327-112,562,327 , GRCh38.p12 chr6: 112,241,126-112,241,126 LAMA4, LAMA4-AS1
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4609717copy number variation1nstd183human GRCh37 chr6: 112,627,640-112,642,326 , GRCh38.p12 chr6: 112,306,438-112,321,124 LAMA4-AS1
    nsv4572965sequence alteration1nstd166human GRCh37.p13 chr6: 112,571,023-112,578,191 , GRCh38.p12 chr6: 112,249,821-112,256,989 LAMA4, LAMA4-AS1
    nsv4549362insertion1nstd166human GRCh37.p13 chr6: 112,563,363-112,563,363 , GRCh38.p12 chr6: 112,242,161-112,242,161 LAMA4-AS1, LAMA4
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