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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975511inversion1nstd209human GRCh38 chr1: 66,986,955-66,987,364 , GRCh37.p13 chr1: 67,452,638-67,453,047 MIER1
    nsv5693497mobile element insertion2nstd211human GRCh38 chr1: 66,950,685-66,950,685 , GRCh37.p13 chr1: 67,416,368-67,416,368 MIER1
    nsv5689894mobile element insertion2nstd211human GRCh38 chr1: 66,958,452-66,958,452 , GRCh37.p13 chr1: 67,424,135-67,424,135 MIER1
    nsv5616512insertion1nstd207human GRCh38 chr1: 66,958,447-66,958,447 , GRCh37.p13 chr1: 67,424,130-67,424,130 MIER1
    nsv5613070insertion1nstd207human GRCh38 chr1: 66,983,527-66,983,527 , GRCh37.p13 chr1: 67,449,210-67,449,210 MIER1
    nsv5543530insertion1nstd206human GRCh38 chr1: 66,950,685-66,950,709 , GRCh37.p13 chr1: 67,416,368-67,416,392 MIER1
    nsv5426915copy number variation1nstd206human GRCh38 chr1: 66,950,671-66,950,733 , GRCh37.p13 chr1: 67,416,354-67,416,416 MIER1
    nsv5425726copy number variation1nstd206human GRCh38 chr1: 66,988,418-66,988,473 , GRCh37.p13 chr1: 67,454,101-67,454,156 MIER1
    nsv5399185mobile element insertion1nstd206human GRCh38 chr1: 66,958,452-66,958,503 , GRCh37.p13 chr1: 67,424,135-67,424,186 MIER1
    nsv5377615translocation1nstd200human GRCh38 chr16: 77,755,046-77,755,046 , GRCh38 chr1: 66,987,666-66,987,666 , GRCh37.p13 chr1: 67,453,349-67,453,349 , GRCh37.p13 chr16: 77,788,943-77,788,943 MIER1, LOC107984878
    nsv5343533translocation1nstd200human GRCh37 chr1: 67,410,134-67,410,134 , GRCh37 chr1: 67,410,076-67,410,076 , GRCh38.p12 chr1: 66,944,393-66,944,393 , GRCh38.p12 chr1: 66,944,451-66,944,451 MIER1
    nsv5330622translocation1nstd200human GRCh37 chr1: 67,452,229-67,452,229 , GRCh37 chr1: 67,452,635-67,452,635 , GRCh38.p12 chr1: 66,986,546-66,986,546 , GRCh38.p12 chr1: 66,986,952-66,986,952 MIER1
    nsv5322072translocation1nstd204human GRCh38.p13 chr1: 66,986,546-66,986,546 , GRCh38.p13 chr1: 66,986,952-66,986,952 , GRCh37.p13 chr1: 67,452,229-67,452,229 , GRCh37.p13 chr1: 67,452,635-67,452,635 MIER1
    nsv5076906mobile element insertion1nstd203human GRCh38 chr1: 66,958,447-66,958,449 , GRCh37.p13 chr1: 67,424,130-67,424,132 MIER1
    nsv5068513mobile element insertion1nstd203human GRCh38 chr1: 66,950,668-66,950,682 , GRCh37.p13 chr1: 67,416,351-67,416,365 MIER1
    nsv5064389mobile element insertion1nstd203human GRCh38 chr1: 66,966,420-66,966,420 , GRCh37.p13 chr1: 67,432,103-67,432,103 MIER1
    nsv4896100copy number variation1nstd200human GRCh38 chr1: 66,963,707-66,969,273 , GRCh37.p13 chr1: 67,429,390-67,434,956 MIER1
    nsv4896099copy number variation1nstd200human GRCh38 chr1: 66,963,036-66,963,920 , GRCh37.p13 chr1: 67,428,719-67,429,603 MIER1
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783565copy number variation1nstd200human GRCh37 chr1: 67,429,390-67,434,956 , GRCh38.p12 chr1: 66,963,707-66,969,273 MIER1
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