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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5430614copy number variation1nstd206human GRCh38 chr1: 26,905,252-26,918,611 , GRCh37.p13 chr1: 27,231,743-27,245,102 NR0B2, NUDC
    nsv5880550copy number variation1nstd209human GRCh38 chr1: 26,908,300-26,914,211 , GRCh37.p13 chr1: 27,234,791-27,240,702 NR0B2, NUDC
    nsv5829935copy number variation1nstd209human GRCh38 chr1: 26,908,332-26,914,231 , GRCh37.p13 chr1: 27,234,823-27,240,722 NR0B2, NUDC
    nsv5829672copy number variation1nstd209human GRCh38 chr1: 26,912,532-26,913,531 , GRCh37.p13 chr1: 27,239,023-27,240,022 NR0B2, NUDC
    nsv5068307mobile element insertion1nstd203human GRCh38 chr1: 26,912,266-26,912,282 , GRCh37.p13 chr1: 27,238,757-27,238,773 NR0B2, NUDC
    nsv5344677translocation1nstd200human GRCh37 chr1: 27,238,541-27,238,541 , GRCh37 chr1: 27,238,444-27,238,444 , GRCh38.p12 chr1: 26,911,953-26,911,953 , GRCh38.p12 chr1: 26,912,050-26,912,050 NR0B2, NUDC
    nsv1195416copy number variation1nstd113human NCBI36 chr1: 27,076,628-27,126,981 , GRCh37.p13 chr1: 27,204,041-27,254,394 , GRCh38.p12 chr1: 26,877,550-26,927,903 NR0B2, NUDC, 2 more genes
    nsv534901copy number variation1nstd54human NCBI36 chr1: 27,076,628-27,126,981 , GRCh37.p13 chr1: 27,204,041-27,254,394 , GRCh38.p12 chr1: 26,877,550-26,927,903 NR0B2, GPN2, 2 more genes
    nsv508689copy number variation1nstd49human NCBI35 chr1: 26,923,095-26,970,139 , GRCh38.p12 chr1: 26,912,462-26,959,506 , GRCh37.p13 chr1: 27,238,953-27,285,997 NR0B2, NUDC, 1 more genes
    nsv3961261insertion1nstd168human GRCh38 chr1: 26,890,608-26,911,705 , GRCh37.p13 chr1: 27,217,099-27,238,196 NR0B2, NUDC, 2 more genes
    nsv3896439copy number variation1nstd102humanPathogenic GRCh38 chr1: 26,807,012-27,685,191 , NCBI36 chr1: 27,006,090-27,884,289 , GRCh37 chr1: 27,133,503-28,011,702 NR0B2, IFI6, 37 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 NR0B2, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 NR0B2, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 NR0B2, RNU1-153P, 4887 more genes
    nsv3901163copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937 NR0B2, TMEM222, 453 more genes
    nsv3898321copy number variation1nstd102humanUncertain significance GRCh38 chr1: 26,854,636-27,645,829 , NCBI36 chr1: 27,053,714-27,844,927 , GRCh37 chr1: 27,181,127-27,972,340 NR0B2, TRNP1, 31 more genes
    nsv429535copy number variation1nstd11human NCBI36 chr1: 21,449,192-32,289,507 , GRCh38.p12 chr1: 21,250,112-32,051,319 , GRCh37.p13 chr1: 21,576,605-32,516,920 NR0B2, ALPL, 305 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 NR0B2, LINC01776, 1853 more genes
    nsv7095609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 25,870,190-27,278,871 , GRCh38.p12 chr1: 25,543,699-26,952,380 NR0B2, RPL34P4, 53 more genes
    nsv3886856copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,119,557-27,547,784 , GRCh38.p12 chr1: 26,793,066-27,221,293 NR0B2, LOC102723760, 19 more genes
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