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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709062mobile element insertion1nstd211human GRCh38 chr15: 43,818,534-43,818,534 , GRCh37.p13 chr15: 44,110,732-44,110,732 MFAP1
    nsv5499036copy number variation1nstd206human GRCh38 chr15: 43,819,598-43,822,397 , GRCh37.p13 chr15: 44,111,796-44,114,595 MFAP1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005330copy number variation1nstd200human GRCh38 chr15: 43,798,223-43,813,836 , GRCh37.p13 chr15: 44,090,421-44,106,034 HYPK, MFAP1, 2 more genes
    nsv5001517copy number variation1nstd200human GRCh38 chr15: 43,819,597-43,822,388 , GRCh37.p13 chr15: 44,111,795-44,114,586 MFAP1
    nsv5001516copy number variation1nstd200human GRCh38 chr15: 43,813,558-43,814,138 , GRCh37.p13 chr15: 44,105,756-44,106,336 MFAP1
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4865957copy number variation1nstd200human GRCh37 chr15: 44,115,319-44,119,998 , GRCh38.p12 chr15: 43,823,121-43,827,800 MFAP1, WDR76
    nsv4865956copy number variation1nstd200human GRCh37 chr15: 44,111,795-44,114,596 , GRCh38.p12 chr15: 43,819,597-43,822,398 MFAP1
    nsv4675221copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,420,601-44,198,616 , GRCh38.p12 chr15: 43,128,403-43,906,418 TGM5, CATSPER2P1, 38 more genes
    nsv4622760copy number variation1nstd183human GRCh37 chr15: 44,093,927-44,104,527 , GRCh38.p12 chr15: 43,801,729-43,812,329 SERF2-C15ORF63, MFAP1, 1 more genes
    nsv4383436copy number variation1nstd173human GRCh37 chr15: 43,851,399-44,325,282 , GRCh38.p12 chr15: 43,559,201-44,033,084 PPIP5K1P1-CATSPER2, RNU6-554P, 24 more genes
    nsv4381260copy number variation1nstd173human GRCh37 chr15: 44,054,738-44,191,082 , GRCh38.p12 chr15: 43,762,540-43,898,884 SERF2-C15ORF63, SERINC4, 9 more genes
    nsv4372500copy number variation1nstd173human GRCh37 chr15: 43,992,627-44,198,616 , GRCh38.p12 chr15: 43,700,429-43,906,418 WDR76, ELL3, 13 more genes
    nsv3961571copy number variation1nstd168human GRCh38 chr15: 43,795,350-43,867,386 , GRCh37.p13 chr15: 44,087,548-44,159,584 MFAP1, SERF2, 4 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
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