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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148042copy number variation1nstd102humanUncertain significance GRCh38 chr1: 12,617,574-12,621,498 , GRCh37.p13 chr1: 12,677,580-12,681,504 DHRS3
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv7049259inversion1nstd229human GRCh38 chr1: 12,588,205-12,588,281 , GRCh37.p13 chr1: 12,648,220-12,648,293 DHRS3
    nsv7048193inversion1nstd229human GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883 PRAMEF36P, HNRNPCL3, 193 more genes
    nsv6657761copy number variation1nstd229human GRCh38 chr1: 9,535,063-15,753,073 , GRCh37.p13 chr1: 9,595,122-16,079,568 SLC25A34-AS1, TMEM274P, 173 more genes
    nsv6641252copy number variation1nstd229human GRCh38 chr1: 12,572,300-12,572,489 , GRCh37.p13 chr1: 12,632,328-12,632,517 DHRS3
    nsv6641138copy number variation1nstd229human GRCh38 chr1: 12,594,481-12,601,461 , GRCh37.p13 chr1: 12,654,494-12,661,473 DHRS3
    nsv6641050copy number variation1nstd229human GRCh38 chr1: 12,609,230-12,614,437 , GRCh37.p13 chr1: 12,669,235-12,674,442 DHRS3
    nsv6641044copy number variation1nstd229human GRCh38 chr1: 12,608,201-12,611,300 , GRCh37.p13 chr1: 12,668,206-12,671,305 DHRS3
    nsv6641041copy number variation1nstd229human GRCh38 chr1: 12,558,801-12,710,900 , GRCh37.p13 chr1: 12,618,831-12,770,902 AADACL4, RNU6ATAC18P, 2 more genes
    nsv6641039copy number variation1nstd229human GRCh38 chr1: 12,538,835-12,629,054 , GRCh37.p13 chr1: 12,598,865-12,689,060 MIR6730, RNU6ATAC18P, 1 more genes
    nsv6640826copy number variation1nstd229human GRCh38 chr1: 12,580,101-12,656,200 , GRCh37.p13 chr1: 12,640,129-12,716,219 DHRS3, AADACL4
    nsv6640825copy number variation1nstd229human GRCh38 chr1: 12,571,283-12,571,475 , GRCh37.p13 chr1: 12,631,311-12,631,503 DHRS3
    nsv6640821copy number variation1nstd229human GRCh38 chr1: 12,466,204-12,655,041 , GRCh37.p13 chr1: 12,526,259-12,715,060 SNORA59A, MIR6730, 5 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6333386copy number variation1nstd223human GRCh38 chr1: 12,538,835-12,629,033 , GRCh37.p13 chr1: 12,598,865-12,689,039 DHRS3, RNU6ATAC18P, 1 more genes
    nsv6326434copy number variation1nstd223human GRCh38 chr1: 12,599,644-12,600,214 , GRCh37.p13 chr1: 12,659,656-12,660,226 DHRS3
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