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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011667copy number variation1nstd229human GRCh37.p13 chr19|NW_003871094.1: 92,969-245,473 , GRCh38 chr19: 8,662,999-8,930,190 , GRCh37.p13 chr19: 8,772,526-8,926,179 MUC16, ZNF558, 5 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv6625466copy number variation1nstd224human GRCh37 chr19: 8,815,355-8,987,218 , GRCh38.p12 chr19: 8,705,006-8,876,542 MBD3L1, RPL23AP78, 3 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5526569copy number variation1nstd206human GRCh38 chr19: 8,345,242-8,989,493 , GRCh37.p13 chr19: 8,410,126-9,100,169 MIR4999, OR2Z1, 16 more genes
    nsv4729804copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,680,063-9,273,676 , GRCh38.p12 chr19: 8,615,177-9,163,000 OR7G1, OR7G2, 14 more genes
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4623652copy number variation2nstd183human GRCh37 chr19: 8,842,850-8,902,156 , GRCh38.p12 chr19: 8,732,489-8,791,480 OR2Z1
    nsv4416179copy number variation1nstd174human GRCh37 chr19: 8,841,687-8,930,139 , GRCh38.p12 chr19: 8,731,325-8,819,463 ZNF558, OR2Z1
    nsv4269019copy number variation1nstd166human GRCh37.p13 chr19: 8,799,185-9,251,695 , GRCh38.p12 chr19: 8,688,936-9,141,019 OR7G15P, OR7G1, 13 more genes
    nsv3971019copy number variation1nstd168human GRCh37.p13 chr19|NW_003871094.1: 158,252-230,303 , GRCh38 chr19: 8,728,282-8,800,333 , GRCh37.p13 chr19: 8,838,644-8,911,009 OR2Z1, RPL23AP78
    nsv3960012insertion1nstd168human GRCh38 chr19: 8,698,925-8,931,204 , GRCh37.p13 chr19: 8,809,275-8,926,179 , GRCh37.p13 chr19|NW_003871094.1: 128,895-245,473 MBD3L1, MUC16, 4 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 SEMA6B, RANBP3-DT, 299 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
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 PCP2, EIF1P6, 250 more genes
    nsv3888397copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059 ELAVL1, MYO1F, 80 more genes
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