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Items: 1 to 20 of 260

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960985insertion1nstd209human GRCh38 chr2: 152,720,034-152,720,034 , GRCh37.p13 chr2: 153,576,548-153,576,548 ARL6IP6
    nsv5903974copy number variation1nstd209human GRCh38 chr2: 152,736,382-152,737,375 , GRCh37.p13 chr2: 153,592,896-153,593,889 ARL6IP6
    nsv5831360copy number variation1nstd209human GRCh38 chr2: 152,736,353-152,737,352 , GRCh37.p13 chr2: 153,592,867-153,593,866 ARL6IP6
    nsv5618161insertion1nstd207human GRCh38 chr2: 152,720,034-152,720,034 , GRCh37.p13 chr2: 153,576,548-153,576,548 ARL6IP6
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 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
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5449059copy number variation1nstd206human GRCh38 chr2: 152,732,205-152,732,267 , GRCh37.p13 chr2: 153,588,719-153,588,781 ARL6IP6
    nsv5448351copy number variation1nstd206human GRCh38 chr2: 151,571,812-153,829,571 , GRCh37.p13 chr2: 152,428,326-154,686,084 , LOC105373691, 20 more genes
    nsv5444636copy number variation1nstd206human GRCh38 chr2: 150,863,589-152,862,185 , GRCh37.p13 chr2: 151,720,103-153,718,699 , CACNB4, 24 more genes
    nsv5440383copy number variation1nstd206human GRCh38 chr2: 152,737,896-152,739,079 , GRCh37.p13 chr2: 153,594,410-153,595,593 ARL6IP6
    nsv5438108copy number variation1nstd206human GRCh38 chr2: 152,720,034-152,720,103 , GRCh37.p13 chr2: 153,576,548-153,576,617 ARL6IP6
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5202600copy number variation1nstd204human GRCh38.p13 chr2: 152,737,753-152,739,052 , GRCh37.p13 chr2: 153,594,267-153,595,566 ARL6IP6
    nsv5200401copy number variation1nstd204human GRCh38.p13 chr2: 152,737,901-152,739,200 , GRCh37.p13 chr2: 153,594,415-153,595,714 ARL6IP6
    nsv5067455mobile element insertion1nstd203human GRCh38 chr2: 152,749,506-152,749,520 , GRCh37.p13 chr2: 153,606,020-153,606,034 ARL6IP6
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4928811copy number variation1nstd200human GRCh38 chr2: 152,759,529-152,829,334 , GRCh37.p13 chr2: 153,616,043-153,685,848 ARL6IP6
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