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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977088insertion1nstd209human GRCh38 chr19: 38,902,085-38,902,085 , GRCh37.p13 chr19: 39,392,725-39,392,725 NFKBIB
    nsv5596919copy number variation1nstd207human GRCh38 chr19: 38,902,484-38,902,565 , GRCh37.p13 chr19: 39,393,124-39,393,205 NFKBIB
    nsv5532569copy number variation1nstd206human GRCh38 chr19: 38,897,545-38,899,097 , GRCh37.p13 chr19: 39,388,185-39,389,737 NFKBIB, SIRT2
    nsv5531153copy number variation1nstd206human GRCh38 chr19: 38,897,330-38,897,988 , GRCh37.p13 chr19: 39,387,970-39,388,628 NFKBIB, SIRT2
    nsv5160248mobile element insertion1nstd203human GRCh38 chr19: 38,902,098-38,902,098 , GRCh37.p13 chr19: 39,392,738-39,392,738 NFKBIB
    nsv4732306copy number variation1nstd199human GRCh37 chr19: 39,393,129-39,393,212 , GRCh38.p12 chr19: 38,902,489-38,902,572 , GRCh38.p12 chr19|NW_014040929.1: 312,161-312,244 NFKBIB
    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
    nsv4440103copy number variation1nstd175human GRCh37 chr19: 39,393,124-39,393,206 , GRCh38.p12 chr19: 38,902,484-38,902,566 , GRCh38.p12 chr19|NW_014040929.1: 312,156-312,238 NFKBIB
    nsv4421469copy number variation1nstd174human GRCh37 chr19: 39,392,960-39,393,490 , GRCh38.p12 chr19: 38,902,320-38,902,850 , GRCh38.p12 chr19|NW_014040929.1: 311,992-312,522 NFKBIB
    nsv4254094copy number variation1nstd166human GRCh37.p13 chr19: 39,388,419-39,389,450 , GRCh38.p12 chr19|NW_014040929.1: 307,451-308,482 , GRCh38.p12 chr19: 38,897,779-38,898,810 NFKBIB, SIRT2
    nsv4252639copy number variation1nstd166human GRCh37.p13 chr19: 39,388,000-39,393,000 , GRCh38.p12 chr19: 38,897,360-38,902,360 , GRCh38.p12 chr19|NW_014040929.1: 307,032-312,032 NFKBIB, SIRT2
    nsv3925328copy number variation1nstd167human GRCh37 chr19: 39,393,124-39,393,206 , GRCh38.p12 chr19: 38,902,484-38,902,566 , GRCh38.p12 chr19|NW_014040929.1: 312,156-312,238 NFKBIB
    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
    nsv3912394copy number variation1nstd102humanUncertain significance NCBI36 chr19: 44,054,509-44,534,649 , GRCh37.p13 chr19: 39,362,669-39,842,809 , GRCh38.p12 chr19: 38,872,029-39,352,169 SAMD4B, IFNL1, 20 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
    nsv3534816copy number variation6nstd152human GRCh38 chr19: 38,902,484-38,902,566 , GRCh37.p13 chr19: 39,393,124-39,393,206 NFKBIB
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