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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908706copy number variation1nstd102humanBenign GRCh37 chr19: 2,422,072-2,444,608 , GRCh38.p12 chr19: 2,422,074-2,444,610 TMPRSS9, TIMM13, 2 more genes
    nsv3890463copy number variation1nstd102humanBenign GRCh37 chr19: 2,422,087-2,444,608 , GRCh38.p12 chr19: 2,422,089-2,444,610 TMPRSS9, TIMM13, 2 more genes
    nsv3910710copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,549,143-4,288,717 , NCBI36 chr19: 1,500,143-4,239,717 , GRCh38 chr19: 1,549,144-4,288,720 TMPRSS9, EBI3, 110 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 TMPRSS9, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 TMPRSS9, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 TMPRSS9, LENG8, 2408 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 TMPRSS9, SEMA6B, 299 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 TMPRSS9, POLR2E, 283 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 TMPRSS9, 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 TMPRSS9, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 TMPRSS9, MRPL54, 198 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 TMPRSS9, AZU1, 159 more genes
    nsv3909324copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,200,875 , GRCh38.p12 chr19: 260,911-3,200,877 TMPRSS9, LOC105372234, 152 more genes
    nsv3915373copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,516,574-4,059,126 , GRCh37 chr19: 1,565,574-4,108,126 , GRCh38 chr19: 1,565,575-4,108,128 TMPRSS9, LOC100419704, 104 more genes
    nsv3921932copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,506,147 , GRCh37 chr19: 259,395-2,555,147 , GRCh38 chr19: 259,395-2,555,149 TMPRSS9, GZMM, 129 more genes
    nsv3895304copy number variation1nstd102humanPathogenic GRCh37 chr19: 277,373-2,555,164 , GRCh38.p12 chr19: 277,373-2,555,166 TMPRSS9, LOC100288123, 129 more genes
    nsv3890661copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 259,395-3,152,419 , GRCh38.p12 chr19: 259,395-3,152,421 TMPRSS9, TLE5, 150 more genes
    nsv3913283copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 372,537-2,848,919 , GRCh37 chr19: 421,537-2,897,919 , GRCh38 chr19: 421,537-2,897,921 TMPRSS9, AMH, 135 more genes
    nsv3902852copy number variation1nstd102humanBenign GRCh37 chr19: 2,422,087-2,477,316 , GRCh38.p12 chr19: 2,422,089-2,477,318 TMPRSS9, LMNB2, 4 more genes
    nsv6637269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,376,834-2,515,283 , GRCh38.p12 chr19: 2,376,836-2,515,285 TMPRSS9, LINC01775, 6 more genes
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