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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5300223copy number variation1nstd204human GRCh38.p13 chr19: 13,638,301-14,767,500 , GRCh37.p13 chr19: 13,749,115-14,878,312 , SNORA104, 53 more genes
    nsv5295552copy number variation1nstd204human GRCh38.p13 chr19: 13,937,101-14,461,200 , GRCh37.p13 chr19: 14,047,914-14,572,012 , ASF1B, 20 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4425330copy number variation1nstd174human GRCh37 chr19: 14,170,554-14,321,100 , GRCh38.p12 chr19: 14,059,742-14,210,288 ADGRL1, ASF1B, 8 more genes
    nsv4341558mobile element insertion1nstd166human GRCh37.p13 chr19: 14,192,451-14,192,451 , GRCh38.p12 chr19: 14,081,639-14,081,639 C19orf67
    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
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3915094copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610 RN7SL619P, ZNF625-ZNF20, 123 more genes
    nsv3913955copy number variation1nstd102humanUncertain significance GRCh37 chr19: 13,644,739-14,369,645 , GRCh38 chr19: 13,533,925-14,258,833 , NCBI36 chr19: 13,505,739-14,230,645 YJU2B, RN7SL619P, 30 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912480copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485 GET3, ADGRE3, 100 more genes
    nsv3910509copy number variation1nstd102humanPathogenic NCBI36 chr19: 13,505,739-15,342,900 , GRCh37 chr19: 13,644,739-15,481,900 , GRCh38 chr19: 13,533,925-15,371,089 DDX39A, SLC1A6, 76 more genes
    nsv3908579copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,124,666-16,431,349 , GRCh38.p12 chr19: 14,013,854-16,320,538 TMEM167AP2, TEKTL1, 99 more genes
    nsv3907864copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385 WDR83, DDX39A, 105 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3899944copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,608,072-14,543,046 , GRCh38.p12 chr19: 11,497,257-14,432,234 RNA5SP465, VN2R14P, 145 more genes
    nsv3898900copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614 FBXL12, DCAF15, 253 more genes
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