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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5288731copy number variation1nstd204human GRCh38.p13 chr19: 41,182,901-41,435,300 , GRCh37.p13 chr19: 41,688,806-41,936,866 LOC105372401, AXL, 13 more genes
    nsv5165573mobile element insertion1nstd203human GRCh38 chr19: 41,313,111-41,313,128 , GRCh37.p13 chr19: 41,819,016-41,819,033 CCDC97
    nsv5020478copy number variation1nstd200human GRCh38 chr19: 41,311,539-41,315,411 , GRCh37.p13 chr19: 41,817,444-41,821,316 CCDC97
    nsv4712685copy number variation1nstd195human GRCh37 chr19: 41,760,751-41,819,601 , GRCh38.p12 chr19: 41,254,846-41,313,696 AXL, HNRNPUL1, 3 more genes
    nsv4676245copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,304,025-41,928,997 , GRCh38.p12 chr19: 40,798,120-41,423,092 CYP2T1P, RN7SL34P, 26 more genes
    nsv4622940copy number variation1nstd183human GRCh37 chr19: 41,770,228-41,815,282 , GRCh38.p12 chr19: 41,264,323-41,309,377 CCDC97, LOC105372401, 2 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4264731copy number variation1nstd166human GRCh37.p13 chr19: 41,825,205-41,825,256 , GRCh38.p12 chr19: 41,319,300-41,319,351 CCDC97
    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
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 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
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
    nsv2752158copy number variation1nstd130human GRCh37 chr19: 289,244-58,996,454 , GRCh38.p12 chr19: 289,244-58,485,087 , NFKBIB, 2456 more genes
    nsv1959994short tandem repeat1nstd128human GRCh37 chr19: 41,825,698-41,825,712 , GRCh38.p12 chr19: 41,319,793-41,319,807 CCDC97
    nsv1959993short tandem repeat7nstd128human GRCh37 chr19: 41,820,885-41,820,901 , GRCh38.p12 chr19: 41,314,980-41,314,996 CCDC97
    nsv1959992short tandem repeat3nstd128human GRCh37 chr19: 41,820,051-41,820,073 , GRCh38.p12 chr19: 41,314,146-41,314,168 CCDC97
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