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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099187copy number variation1nstd231human GRCh38.p12 chr1: 24,354,009-27,158,528 , GRCh37 chr1: 24,680,499-27,485,019 RUNX3, CD52, 88 more genes
    nsv7095609copy number variation1nstd102humanUncertain significance GRCh37 chr1: 25,870,190-27,278,871 , GRCh38.p12 chr1: 25,543,699-26,952,380 RPL34P4, GPATCH3, 53 more genes
    nsv7041935inversion1nstd229human GRCh38 chr1: 26,508,472-26,804,965 , GRCh37.p13 chr1: 26,834,963-27,131,456 MIR1976, LOC101928728, 6 more genes
    nsv6648045copy number variation1nstd229human GRCh38 chr1: 26,400,001-27,138,900 , GRCh37.p13 chr1: 26,726,492-27,465,391 RN7SL679P, NR0B2, 26 more genes
    nsv6647354copy number variation1nstd229human GRCh38 chr1: 26,095,901-27,680,900 , GRCh37.p13 chr1: 26,422,392-28,007,411 ZPLD2P, CEP85, 65 more genes
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6333556copy number variation1nstd223human GRCh38 chr1: 24,890,501-27,921,300 , GRCh37.p13 chr1: 25,216,992-28,247,811 RUNX3, MACO1, 108 more genes
    nsv6318166copy number variation1nstd223human GRCh38 chr1: 26,688,492-26,690,115 , GRCh37.p13 chr1: 27,014,983-27,016,606 LOC101928728, LOC105376888
    nsv6290421copy number variation1nstd102humanUncertain significance GRCh37 chr1: 26,246,213-27,044,118 , GRCh38.p12 chr1: 25,919,722-26,717,627 C1orf232, CEP85, 32 more genes
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv6112710copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr1: 26,675,007-26,783,840 , GRCh37 chr1: 27,001,498-27,110,331 ARID1A, LOC101928728, 1 more genes
    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
    nsv5219260copy number variation1nstd204human GRCh38.p13 chr1: 26,596,401-26,818,700 , GRCh37.p13 chr1: 26,922,892-27,145,191 LOC105376888, PIGV, 3 more genes
    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
    nsv4460800mobile element insertion1nstd166human GRCh37.p13 chr1: 27,021,082-27,021,082 , GRCh38.p12 chr1: 26,694,591-26,694,591 LOC101928728, ARID1A
    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
    nsv4326321sequence alteration1nstd166human GRCh38.p12 chr1: 26,508,516-26,804,975 , GRCh37.p13 chr1: 26,835,007-27,131,466 , GRCh38.p12 chr1|NW_009646195.1: 1-166,200 RPS6KA1, ARID1A, 6 more genes
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