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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902464copy number variation1nstd209human GRCh38 chr2: 159,716,557-159,716,628 , GRCh37.p13 chr2: 160,573,068-160,573,139 MARCHF7
    nsv5891190copy number variation1nstd209human GRCh38 chr2: 159,730,998-159,733,491 , GRCh37.p13 chr2: 160,587,509-160,590,002 MARCHF7
    nsv5831898copy number variation1nstd209human GRCh38 chr2: 159,745,185-159,746,662 , GRCh37.p13 chr2: 160,601,696-160,603,173 MARCHF7
    nsv5831696copy number variation1nstd209human GRCh38 chr2: 159,731,459-159,733,538 , GRCh37.p13 chr2: 160,587,970-160,590,049 MARCHF7
    nsv5831695copy number variation1nstd209human GRCh38 chr2: 159,731,009-159,734,238 , GRCh37.p13 chr2: 160,587,520-160,590,749 MARCHF7
    nsv5682187mobile element insertion2nstd211human GRCh38 chr2: 159,767,034-159,767,034 , GRCh37.p13 chr2: 160,623,545-160,623,545 CD302, MARCHF7, 1 more genes
    nsv5677980mobile element insertion2nstd211human GRCh38 chr2: 159,746,193-159,746,193 , GRCh37.p13 chr2: 160,602,704-160,602,704 MARCHF7
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5560575sequence alteration1nstd206human GRCh38 chr2: 159,316,539-159,936,193 , GRCh37.p13 chr2: 160,173,050-160,792,704 LY75, CD302, 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
    nsv5546440insertion1nstd206human GRCh38 chr2: 159,717,646-159,717,679 , GRCh37.p13 chr2: 160,574,157-160,574,190 MARCHF7
    nsv5534651insertion1nstd206human GRCh38 chr2: 159,767,034-159,767,070 , GRCh37.p13 chr2: 160,623,545-160,623,581 CD302, MARCHF7, 1 more genes
    nsv5451611copy number variation1nstd206human GRCh38 chr2: 159,731,001-159,733,492 , GRCh37.p13 chr2: 160,587,512-160,590,003 MARCHF7
    nsv5442064copy number variation1nstd206human GRCh38 chr2: 159,766,505-159,766,577 , GRCh37.p13 chr2: 160,623,016-160,623,088 MARCHF7
    nsv5440708copy number variation1nstd206human GRCh38 chr2: 159,737,385-159,737,488 , GRCh37.p13 chr2: 160,593,896-160,593,999 MARCHF7
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5350909translocation1nstd200human GRCh38 chr2: 159,713,668-159,713,668 , GRCh38 chr2: 159,713,606-159,713,606 , GRCh37.p13 chr2: 160,570,117-160,570,117 , GRCh37.p13 chr2: 160,570,179-160,570,179 MARCHF7
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5211243copy number variation1nstd204human GRCh38.p13 chr2: 159,726,505-159,751,164 , GRCh37.p13 chr2: 160,583,016-160,607,675 MARCHF7
    nsv5078611mobile element insertion1nstd203human GRCh38 chr2: 159,746,180-159,746,193 , GRCh37.p13 chr2: 160,602,691-160,602,704 MARCHF7
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