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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5709183mobile element insertion1nstd211human GRCh38 chr19: 11,551,193-11,551,193 , GRCh37.p13 chr19: 11,662,008-11,662,008 ELOF1
    nsv5531608copy number variation1nstd206human GRCh38 chr19: 11,554,611-11,557,738 , GRCh37.p13 chr19: 11,665,426-11,668,553 ELOF1
    nsv5520665copy number variation1nstd206human GRCh38 chr19: 11,557,350-11,557,419 , GRCh37.p13 chr19: 11,668,165-11,668,234 ELOF1
    nsv5418266mobile element insertion1nstd206human GRCh38 chr19: 11,551,193-11,551,244 , GRCh37.p13 chr19: 11,662,008-11,662,059 ELOF1
    nsv5298909copy number variation1nstd204human GRCh38.p13 chr19: 10,842,201-11,593,800 , GRCh37.p13 chr19: 10,952,877-11,704,615 KANK2, RPL18AP13, 35 more genes
    nsv5295569copy number variation1nstd204human GRCh38.p13 chr19: 11,293,101-11,613,000 , GRCh37.p13 chr19: 11,403,777-11,723,815 ELAVL3, ACP5, 21 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5171140mobile element insertion1nstd203human GRCh38 chr19: 11,551,180-11,551,193 , GRCh37.p13 chr19: 11,661,995-11,662,008 ELOF1
    nsv5011702copy number variation1nstd200human GRCh38 chr19: 11,557,761-11,561,746 , GRCh37.p13 chr19: 11,668,576-11,672,561 ELOF1
    nsv5011701copy number variation1nstd200human GRCh38 chr19: 11,554,843-11,557,740 , GRCh37.p13 chr19: 11,665,658-11,668,555 ELOF1
    nsv4729806copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,957,601-11,672,041 , GRCh38.p12 chr19: 10,846,925-11,561,226 DOCK6-AS1, C19orf38, 32 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676222copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,445,773-12,160,664 , GRCh38.p12 chr19: 11,335,097-12,049,849 ECSIT, MIR7974, 41 more genes
    nsv4676174copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,667,844-11,780,171 , GRCh38.p12 chr19: 11,557,029-11,669,356 ACP5, VN2R12P, 5 more genes
    nsv4500984mobile element insertion1nstd166human GRCh37.p13 chr19: 11,661,995-11,661,995 , GRCh38.p12 chr19: 11,551,180-11,551,180 ELOF1
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
    nsv4392281copy number variation1nstd171human GRCh37 chr19: 11,668,164-11,668,234 , GRCh38.p12 chr19: 11,557,349-11,557,419 ELOF1
    nsv3960925copy number variation1nstd168human GRCh38 chr19: 11,513,686-11,558,109 , GRCh37.p13 chr19: 11,624,501-11,668,924 CNN1, ECSIT, 4 more genes
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
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