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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5287129copy number variation1nstd204human GRCh38.p13 chr19: 40,119,401-40,793,500 , GRCh37.p13 chr19: 40,625,308-41,299,405 CCNP, SHKBP1, 28 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
    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
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3895039copy number variation1nstd102humanBenign GRCh37 chr19: 40,636,400-41,060,616 , GRCh38.p12 chr19: 40,130,493-40,554,710 MIR6796, PLD3, 15 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
    nsv3158935copy number variation1nstd151human GRCh37 chr19: 40,405,916-41,111,135 , GRCh38.p12 chr19: 39,906,247-40,605,229 , MIR6796, 26 more genes
    nsv2785371copy number variation1nstd132human NCBI36 chr19: 45,283,022-45,990,855 , GRCh37.p13 chr19: 40,591,182-41,299,015 , GRCh38.p12 chr19: 40,085,275-40,793,110 MAP3K10, RAB4B, 29 more genes
    nsv2764236copy number variation1nstd130human NCBI36 chr19: 45,516,128-46,314,029 , GRCh37.p13 chr19: 40,824,288-41,622,189 , GRCh38.p12 chr19: 40,318,381-41,116,284 , SERTAD3-AS1, 33 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
    nsv1959099short tandem repeat6nstd128human GRCh37 chr19: 40,928,163-40,928,180 , GRCh38.p12 chr19: 40,422,256-40,422,273 SERTAD1
    nsv1958877short tandem repeat1nstd128human GRCh37 chr19: 40,929,404-40,929,424 , GRCh38.p12 chr19: 40,423,497-40,423,517 SERTAD1
    nsv1958876short tandem repeat3nstd128human GRCh37 chr19: 40,927,761-40,927,773 , GRCh38.p12 chr19: 40,421,854-40,421,866 SERTAD1
    nsv1958875short tandem repeat1nstd128human GRCh37 chr19: 40,926,380-40,926,405 , GRCh38.p12 chr19: 40,420,473-40,420,498 SERTAD1
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