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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880550copy number variation1nstd209human GRCh38 chr1: 26,908,300-26,914,211 , GRCh37.p13 chr1: 27,234,791-27,240,702 NUDC, NR0B2
    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 NUDC, NR0B2
    nsv5430614copy number variation1nstd206human GRCh38 chr1: 26,905,252-26,918,611 , GRCh37.p13 chr1: 27,231,743-27,245,102 NUDC, NR0B2
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    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
    nsv5206193copy number variation1nstd204human GRCh38.p13 chr1: 26,819,201-27,230,300 , GRCh37.p13 chr1: 27,145,692-27,556,791 KDF1, RPL12P13, 18 more genes
    nsv5068307mobile element insertion1nstd203human GRCh38 chr1: 26,912,266-26,912,282 , GRCh37.p13 chr1: 27,238,757-27,238,773 NUDC, NR0B2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4580966copy number variation1nstd183human GRCh37 chr1: 27,039,290-27,468,019 , GRCh38.p12 chr1: 26,712,799-27,141,528 GPN2, ARID1A, 15 more genes
    nsv4517994copy number variation1nstd166human GRCh37.p13 chr1: 27,175,760-27,426,678 , GRCh38.p12 chr1: 26,849,269-27,100,187 SFN, OSTCP2, 12 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4313420sequence alteration1nstd166human GRCh37.p13 chr1: 27,089,972-27,281,573 , GRCh38.p12 chr1: 26,763,481-26,955,082 ARID1A, SFN, 8 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
    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 TMEM222, ZBTB8OS, 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
    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 IFI6, FGR, 37 more genes
    nsv3886856copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,119,557-27,547,784 , GRCh38.p12 chr1: 26,793,066-27,221,293 LOC102723760, NPM1P39, 19 more genes
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