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Items: 1 to 20 of 45

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891494copy number variation1nstd102humanBenign GRCh37 chr19: 1,248,201-1,250,885 , GRCh38.p12 chr19: 1,248,202-1,250,886 MIDN, LOC102723811
    nsv3893093copy number variation1nstd102humanBenign GRCh37 chr19: 1,241,594-1,250,885 , GRCh38.p12 chr19: 1,241,595-1,250,886 MIDN, ATP5F1D, 1 more genes
    nsv3897821copy number variation1nstd102humanBenign GRCh37 chr19: 1,242,574-1,250,885 , GRCh38.p12 chr19: 1,242,575-1,250,886 MIDN, LOC102723811, 1 more genes
    nsv3900174copy number variation1nstd102humanBenign GRCh37 chr19: 1,218,523-1,257,027 , GRCh38.p12 chr19: 1,218,524-1,257,028 MIDN, STK11, 3 more genes
    nsv3893242copy number variation1nstd102humanBenign GRCh37 chr19: 1,221,319-1,257,027 , GRCh38.p12 chr19: 1,221,320-1,257,028 MIDN, LOC102723811, 3 more genes
    nsv6315510copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-1,319,319 , GRCh38.p12 chr19: 260,911-1,319,320 MIDN, LOC101928450, 66 more genes
    nsv3922151copy number variation1nstd102humanPathogenic NCBI36 chr19: 896,098-1,923,298 , GRCh38 chr19: 945,098-1,972,299 , GRCh37 chr19: 945,098-1,972,298 MIDN, MIR1909, 58 more genes
    nsv3916147copy number variation1nstd102humanPathogenic GRCh37 chr19: 786,550-1,297,499 , GRCh38 chr19: 786,550-1,297,500 , NCBI36 chr19: 737,550-1,248,499 MIDN, LOC102725180, 36 more genes
    nsv7095264copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,913-1,650,247 , GRCh38.p12 chr19: 1,206,914-1,650,248 MIDN, NDUFS7, 30 more genes
    nsv3909124copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,119,019-1,451,274 , GRCh38.p12 chr19: 1,119,020-1,451,275 MIDN, APC2, 22 more genes
    nsv6637184copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,205,244-1,479,188 , GRCh38.p12 chr19: 1,205,245-1,479,189 MIDN, C19orf25, 19 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 MIDN, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 MIDN, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 MIDN, LENG8, 2408 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 MIDN, POLR2E, 283 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 MIDN, BSG, 217 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 MIDN, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MIDN, MRPL54, 198 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 MIDN, AZU1, 159 more genes
    nsv3909324copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,200,875 , GRCh38.p12 chr19: 260,911-3,200,877 MIDN, LOC105372234, 152 more genes
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