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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5889110copy number variation1nstd209human GRCh38 chr5: 43,484,166-43,486,919 , GRCh37.p13 chr5: 43,484,268-43,487,021 TMEM267, C5orf34, 1 more genes
    nsv5842731copy number variation1nstd209human GRCh38 chr5: 43,484,122-43,486,496 , GRCh37.p13 chr5: 43,484,224-43,486,598 TMEM267, C5orf34, 1 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5320035copy number variation1nstd204human GRCh37.p13 chr5: 43,503,795-43,504,121 , GRCh38.p13 chr5: 43,503,693-43,504,019 C5orf34, C5orf34-AS1
    nsv5219871mobile element deletion1nstd204human GRCh37.p13 chr5: 43,512,860-43,513,189 , GRCh38.p13 chr5: 43,512,758-43,513,087 C5orf34-AS1, C5orf34
    nsv5190717mobile element insertion1nstd203human GRCh38 chr5: 43,509,492-43,509,509 , GRCh37.p13 chr5: 43,509,594-43,509,611 C5orf34, C5orf34-AS1
    nsv4944651copy number variation1nstd200human GRCh38 chr5: 43,509,998-43,529,686 , GRCh37.p13 chr5: 43,510,100-43,529,788 C5orf34-AS1, C5orf34, 1 more genes
    nsv4778313mobile element deletion1nstd200human GRCh37 chr5: 43,512,869-43,513,181 , GRCh38.p12 chr5: 43,512,767-43,513,079 C5orf34-AS1, C5orf34
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
    nsv4591157copy number variation1nstd183human GRCh37 chr5: 43,490,521-43,491,080 , GRCh38.p12 chr5: 43,490,419-43,490,978 C5orf34-AS1, C5orf34
    nsv4563142mobile element insertion1nstd166human GRCh37.p13 chr5: 43,509,594-43,509,594 , GRCh38.p12 chr5: 43,509,492-43,509,492 C5orf34, C5orf34-AS1
    nsv4523416copy number variation1nstd166human GRCh37.p13 chr5: 43,511,213-43,511,317 , GRCh38.p12 chr5: 43,511,111-43,511,215 C5orf34, C5orf34-AS1
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
    nsv4456588copy number variation1nstd102humanUncertain significance GRCh37 chr5: 43,383,397-43,687,730 , GRCh38.p12 chr5: 43,383,295-43,687,628 NNT-AS1, AMD1P3, 8 more genes
    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
    nsv4383093copy number variation1nstd173human GRCh37 chr5: 43,414,519-43,499,486 , GRCh38.p12 chr5: 43,414,417-43,499,384 C5orf34, TMEM267, 2 more genes
    nsv4378580copy number variation1nstd173human GRCh37 chr5: 43,416,980-43,499,486 , GRCh38.p12 chr5: 43,416,878-43,499,384 C5orf34, TMEM267, 2 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
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