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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959371insertion1nstd209human GRCh38 chr5: 77,041,788-77,041,788 , GRCh37.p13 chr5: 76,337,613-76,337,613 AGGF1
    nsv5685390mobile element insertion1nstd211human GRCh38 chr5: 77,039,428-77,039,428 , GRCh37.p13 chr5: 76,335,253-76,335,253 AGGF1
    nsv5685223mobile element insertion2nstd211human GRCh38 chr5: 77,032,274-77,032,274 , GRCh37.p13 chr5: 76,328,099-76,328,099 AGGF1
    nsv5637326insertion1nstd207human GRCh38 chr5: 77,042,346-77,042,346 , GRCh37.p13 chr5: 76,338,171-76,338,171 AGGF1
    nsv5634350insertion1nstd207human GRCh38 chr5: 77,043,528-77,043,528 , GRCh37.p13 chr5: 76,339,353-76,339,353 AGGF1
    nsv5580763copy number variation1nstd207human GRCh38 chr5: 77,042,480-77,042,671 , GRCh37.p13 chr5: 76,338,305-76,338,496 AGGF1
    nsv5580720copy number variation1nstd207human GRCh38 chr5: 77,042,787-77,042,932 , GRCh37.p13 chr5: 76,338,612-76,338,757 AGGF1
    nsv5579864copy number variation1nstd207human GRCh38 chr5: 77,042,651-77,043,199 , GRCh37.p13 chr5: 76,338,476-76,339,024 AGGF1
    nsv5573492copy number variation1nstd207human GRCh38 chr5: 77,043,355-77,043,481 , GRCh37.p13 chr5: 76,339,180-76,339,306 AGGF1
    nsv5408104mobile element insertion1nstd206human GRCh38 chr5: 77,039,428-77,039,479 , GRCh37.p13 chr5: 76,335,253-76,335,304 AGGF1
    nsv5091264mobile element insertion1nstd203human GRCh38 chr5: 77,063,386-77,063,400 , GRCh37.p13 chr5: 76,359,211-76,359,225 AGGF1
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4750006copy number variation1nstd199human GRCh37 chr5: 76,338,247-76,338,301 , GRCh38.p12 chr5: 77,042,422-77,042,476 AGGF1
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4591595copy number variation1nstd183human GRCh37 chr5: 76,088,861-76,547,813 , GRCh38.p12 chr5: 76,793,036-77,251,988 ZBED3-AS1, SNORA47, 9 more genes
    nsv4566489mobile element insertion1nstd166human GRCh37.p13 chr5: 76,337,606-76,337,606 , GRCh38.p12 chr5: 77,041,781-77,041,781 AGGF1
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4409411copy number variation1nstd174human GRCh37 chr5: 76,190,936-76,414,733 , GRCh38.p12 chr5: 76,895,111-77,118,908 CRHBP, AGGF1, 5 more genes
    nsv4398381copy number variation1nstd174human GRCh37 chr5: 76,316,147-76,324,734 , GRCh38.p12 chr5: 77,020,322-77,028,909 AGGF1
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
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