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Items: 1 to 20 of 361

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978109inversion1nstd209human GRCh38 chr19: 54,222,352-54,696,988 , GRCh37.p13 chr19|NW_004166865.1: 196,719-671,355 LAIR1, LAIR2, 29 more genes
    nsv5973594insertion1nstd209human GRCh38 chr19: 54,250,278-54,250,278 , GRCh37.p13 chr19|NW_004166865.1: 224,645-224,645 LILRB5
    nsv5701348mobile element insertion2nstd211human GRCh38 chr19: 54,250,292-54,250,292 , GRCh37.p13 chr19|NW_004166865.1: 224,659-224,659 LILRB5
    nsv5521170copy number variation1nstd206human GRCh38 chr19: 54,220,538-54,336,889 , GRCh37.p13 chr19|NW_004166865.1: 194,905-311,256 LILRA4, MIR4752, 10 more genes
    nsv5416718mobile element insertion1nstd206human GRCh38 chr19: 54,250,292-54,250,343 , GRCh37.p13 chr19|NW_004166865.1: 224,659-224,710 LILRB5
    nsv5324812copy number variation1nstd204human GRCh38.p13 chr19: 54,220,162-54,337,386 , GRCh37.p13 chr19|NW_004166865.1: 194,529-311,753 LOC100421130, LILRA6, 10 more genes
    nsv5299210copy number variation1nstd204human GRCh38.p13 chr19: 54,243,895-54,280,137 , GRCh37.p13 chr19|NW_004166865.1: 218,262-254,504 LOC100420187, LILRB2, 3 more genes
    nsv5293304copy number variation1nstd204human GRCh38.p13 chr19: 54,244,794-54,247,851 , GRCh37.p13 chr19|NW_004166865.1: 219,161-222,218 LILRB5
    nsv5288289copy number variation1nstd204human GRCh38.p13 chr19: 54,240,801-54,349,500 , GRCh37.p13 chr19|NW_004166865.1: 215,168-323,867 RNU6-1307P, LOC100420187, 8 more genes
    nsv5282186copy number variation1nstd204human GRCh38.p13 chr19: 54,245,169-54,251,954 , GRCh37.p13 chr19|NW_004166865.1: 219,536-226,321 LILRB5
    nsv5175344mobile element insertion1nstd203human GRCh38 chr19: 54,250,278-54,250,288 , GRCh37.p13 chr19|NW_004166865.1: 224,645-224,655 LILRB5
    nsv5169158mobile element insertion1nstd203human GRCh38 chr19: 54,250,281-54,250,289 , GRCh37.p13 chr19|NW_004166865.1: 224,648-224,656 LILRB5
    nsv5024925copy number variation1nstd200human GRCh38 chr19: 54,248,863-54,249,833 , GRCh37.p13 chr19|NW_004166865.1: 223,230-224,200 LILRB5
    nsv5024923copy number variation1nstd200human GRCh38 chr19: 54,208,427-54,305,909 , GRCh37.p13 chr19|NW_004166865.1: 182,794-280,276 LOC100420187, LILRB2, 8 more genes
    nsv5021329copy number variation1nstd200human GRCh38 chr19: 54,249,996-54,253,015 , GRCh37.p13 chr19|NW_004166865.1: 224,363-227,382 LILRB5
    nsv4861342copy number variation1nstd200human GRCh37 chr19: 54,753,882-54,756,853 , GRCh38.p12 chr19: 54,250,023-54,252,990 , GRCh38.p12 chr19|NT_187693.1: 224,996-227,967 , GRCh38.p12 chr19|NW_003571061.2: 225,027-227,993 , GRCh38.p12 chr19|NW_003571060.1: 224,991-227,958 , GRCh38.p12 chr19|NW_003571054.1: 224,758-227,725 LILRB5
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 KIR3DP1, NLRP9, 133 more genes
    nsv4729999copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,659,105-54,916,280 , GRCh38.p12 chr19|NT_187693.1: 134,805-387,394 , GRCh38.p12 chr19|NW_003571054.1: 130,217-309,793 , GRCh38.p12 chr19: 54,155,367-54,404,676 , GRCh38.p12 chr19|NW_003571061.2: 130,218-361,078 , GRCh38.p12 chr19|NW_003571060.1: 130,218-309,667 , GRCh38.p12 chr19|NW_003571055.2: 134,805-385,761 RPS9, MIR4752, 23 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4725263insertion1nstd186human GRCh37 chr19: 54,754,142-54,754,142 , GRCh38.p12 chr19|NW_003571060.1: 225,246-225,246 , GRCh38.p12 chr19|NT_187693.1: 225,256-225,256 , GRCh38.p12 chr19|NW_003571061.2: 225,282-225,282 , GRCh38.p12 chr19|NW_003571054.1: 225,013-225,013 , GRCh38.p12 chr19: 54,250,278-54,250,278 LILRB5
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