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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933923copy number variation1nstd209human GRCh38 chr17: 44,036,338-44,036,930 , GRCh37.p13 chr17: 42,113,706-42,114,298 LSM12
    nsv5885735copy number variation1nstd209human GRCh38 chr17: 44,048,431-44,051,630 , GRCh37.p13 chr17: 42,125,799-42,128,998 LSM12
    nsv5880948copy number variation1nstd209human GRCh38 chr17: 44,048,581-44,053,367 , GRCh37.p13 chr17: 42,125,949-42,130,735 LSM12
    nsv5877592copy number variation1nstd209human GRCh38 chr17: 44,035,773-44,037,110 , GRCh37.p13 chr17: 42,113,141-42,114,478 LSM12
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5529280copy number variation1nstd206human GRCh38 chr17: 44,042,690-44,045,153 , GRCh37.p13 chr17: 42,120,058-42,122,521 LSM12
    nsv5527966copy number variation1nstd206human GRCh38 chr17: 44,056,762-44,057,484 , GRCh37.p13 chr17: 42,134,130-42,134,852 LSM12
    nsv5526986copy number variation1nstd206human GRCh38 chr17: 44,064,292-44,064,953 , GRCh37.p13 chr17: 42,141,660-42,142,321 LSM12
    nsv5522972copy number variation1nstd206human GRCh38 chr17: 44,042,560-44,045,561 , GRCh37.p13 chr17: 42,119,928-42,122,929 LSM12
    nsv5520327copy number variation1nstd206human GRCh38 chr17: 44,045,087-44,047,256 , GRCh37.p13 chr17: 42,122,455-42,124,624 LSM12
    nsv5328325copy number variation1nstd204human GRCh38.p13 chr17: 44,042,677-44,045,134 , GRCh37.p13 chr17: 42,120,045-42,122,502 LSM12
    nsv5294295copy number variation1nstd204human GRCh38.p13 chr17: 44,042,701-44,045,100 , GRCh37.p13 chr17: 42,120,069-42,122,468 LSM12
    nsv5156184mobile element insertion1nstd203human GRCh38 chr17: 44,033,755-44,033,768 , GRCh37.p13 chr17: 42,111,123-42,111,136 LSM12
    nsv5016502copy number variation1nstd200human GRCh38 chr17: 44,058,671-44,062,682 , GRCh37.p13 chr17: 42,136,039-42,140,050 LSM12
    nsv5016501copy number variation1nstd200human GRCh38 chr17: 44,058,163-44,060,048 , GRCh37.p13 chr17: 42,135,531-42,137,416 LSM12
    nsv5016500copy number variation1nstd200human GRCh38 chr17: 44,056,919-44,060,037 , GRCh37.p13 chr17: 42,134,287-42,137,405 LSM12
    nsv5016499copy number variation1nstd200human GRCh38 chr17: 44,056,762-44,057,484 , GRCh37.p13 chr17: 42,134,130-42,134,852 LSM12
    nsv5016498copy number variation1nstd200human GRCh38 chr17: 44,045,136-44,047,262 , GRCh37.p13 chr17: 42,122,504-42,124,630 LSM12
    nsv5016497copy number variation1nstd200human GRCh38 chr17: 44,042,731-44,047,336 , GRCh37.p13 chr17: 42,120,099-42,124,704 LSM12
    nsv5016496copy number variation1nstd200human GRCh38 chr17: 44,042,677-44,045,132 , GRCh37.p13 chr17: 42,120,045-42,122,500 LSM12
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