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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5720446mobile element insertion1nstd211human GRCh38 chr19: 40,215,623-40,215,623 , GRCh37.p13 chr19: 40,721,530-40,721,530 MAP3K10, TTC9B
    nsv5558284sequence alteration1nstd206human GRCh38 chr19: 40,171,920-40,325,062 , GRCh37.p13 chr19: 40,677,827-40,830,969 AKT2, MAP3K10, 6 more genes
    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
    nsv3161897copy number variation1nstd151human GRCh37 chr19: 40,704,279-40,829,988 , GRCh38.p12 chr19: 40,198,372-40,324,081 LOC107985289, CCNP, 6 more genes
    nsv3160612copy number variation1nstd151human GRCh37 chr19: 40,711,815-40,723,281 , GRCh38.p12 chr19: 40,205,908-40,217,374 MAP3K10, TTC9B
    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
    esv3883798copy number variation1estd219human GRCh37 chr19: 40,696,966-40,834,492 , GRCh38.p12 chr19: 40,191,059-40,328,585 AKT2, MAP3K10, 6 more genes
    esv3883799copy number variation1estd219human GRCh37 chr19: 40,709,031-40,794,619 , GRCh38.p12 chr19: 40,203,124-40,288,712 AKT2, MAP3K10, 4 more genes
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
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