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Items: 1 to 20 of 377

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5670092inversion1nstd207human GRCh38 chr2: 87,362,763-87,699,046 , GRCh37.p13 chr2: 87,589,886-87,998,565 , PAFAH1B1P1, 7 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5443425copy number variation1nstd206human GRCh38 chr2: 87,407,619-87,712,809 , GRCh37.p13 chr2: 87,634,742-88,012,328 , PAFAH1B1P1, 7 more genes
    nsv5440303copy number variation1nstd206human GRCh38 chr2: 87,133,619-87,703,809 , GRCh37.p13 chr2: 87,360,742-88,003,328 , CYTOR, 17 more genes
    nsv5439081copy number variation1nstd206human GRCh38 chr2: 87,622,619-87,719,619 , GRCh37.p13 chr2: 87,922,138-88,019,138 ANAPC1P4, MIR4435-1, 2 more genes
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5219052copy number variation1nstd204human GRCh38.p13 chr2: 87,619,801-87,664,200 , GRCh37.p13 chr2: 87,919,320-87,963,719 RPS14P5, LOC101928214, 1 more genes
    nsv5211677copy number variation1nstd204human GRCh38.p13 chr2: 87,626,001-87,637,800 , GRCh37.p13 chr2: 87,925,520-87,937,319 MIR4435-1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4680880copy number variation1nstd189human GRCh37.p13 chr2: 87,287,602-87,996,372 , GRCh38.p12 chr2: 87,060,479-87,696,853 , PAFAH1B1P1, 20 more genes
    nsv4680424copy number variation1nstd189human GRCh37.p13 chr2: 87,322,043-88,024,667 , GRCh38.p12 chr2: 87,094,920-87,725,148 , PAFAH1B1P1, 20 more genes
    nsv4680384copy number variation1nstd189human GRCh37.p13 chr2: 87,297,291-88,052,330 , GRCh38.p12 chr2: 87,070,168-87,752,811 , PLGLB2, 22 more genes
    nsv4680049copy number variation1nstd189human GRCh37.p13 chr2: 87,250,497-88,052,330 , GRCh38.p12 chr2: 87,023,374-87,752,811 , PLGLB2, 22 more genes
    nsv4679934copy number variation1nstd189human GRCh37.p13 chr2: 87,120,496-88,024,667 , GRCh38.p12 chr2: 86,893,373-87,725,148 , PLGLB1, 26 more genes
    nsv4679670copy number variation1nstd189human GRCh37.p13 chr2: 87,250,497-87,996,372 , GRCh38.p12 chr2: 87,023,374-87,696,853 , PAFAH1B1P1, 20 more genes
    nsv4679426copy number variation1nstd189human GRCh37.p13 chr2: 87,322,043-88,052,330 , GRCh38.p12 chr2: 87,094,920-87,752,811 , PLGLB2, 21 more genes
    nsv4679184copy number variation1nstd189human GRCh37.p13 chr2: 87,306,949-88,052,330 , GRCh38.p12 chr2: 87,079,826-87,752,811 , PLGLB2, 21 more genes
    nsv4668166copy number variation1nstd186human GRCh37 chr2: 87,928,699-87,997,635 , GRCh38.p12 chr2: 87,629,180-87,698,116 RPS14P5, MIR4435-1, 1 more genes
    nsv4663386copy number variation1nstd186human GRCh37 chr2: 87,159,729-88,004,998 , GRCh38.p12 chr2: 86,932,606-87,705,479 , PAFAH1B1P1, 24 more genes
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