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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv7040370inversion1nstd229human GRCh38 chr1: 28,324,061-28,688,380 , GRCh37.p13 chr1: 28,650,572-29,014,892 PHACTR4, SNORD99, 17 more genes
    nsv6648334copy number variation1nstd229human GRCh38 chr1: 28,576,199-28,658,409 , GRCh37.p13 chr1: 28,902,711-28,984,921 SNORA61, TAF12-DT, 8 more genes
    nsv6648307copy number variation1nstd229human GRCh38 chr1: 28,647,644-28,650,322 , GRCh37.p13 chr1: 28,974,156-28,976,834 TAF12-DT, RNU11, 1 more genes
    nsv6648160copy number variation1nstd229human GRCh38 chr1: 28,455,818-28,753,520 , GRCh37.p13 chr1: 28,782,329-29,080,032 GMEB1, YTHDF2, 17 more genes
    nsv6335106copy number variation1nstd223human GRCh38 chr1: 28,644,061-28,647,809 , GRCh37.p13 chr1: 28,970,573-28,974,321 TAF12, TAF12-DT, 1 more genes
    nsv6319572copy number variation1nstd223human GRCh38 chr1: 28,455,818-28,753,520 , GRCh37.p13 chr1: 28,782,329-29,080,032 RAB42, SNORA44, 17 more genes
    nsv6318371copy number variation1nstd223human GRCh38 chr1: 28,647,644-28,650,322 , GRCh37.p13 chr1: 28,974,156-28,976,834 RNU11, TAF12-DT, 1 more genes
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6290388copy number variation1nstd102humanUncertain significance GRCh37 chr1: 28,493,687-29,242,679 , GRCh38.p12 chr1: 28,167,176-28,916,167 SNORA16A, MED18, 24 more genes
    nsv5212241copy number variation1nstd204human GRCh38.p13 chr1: 28,084,401-28,971,400 , GRCh37.p13 chr1: 28,410,912-29,297,912 SNORA73B, ARL8BP2, 29 more genes
    nsv5208686copy number variation1nstd204human GRCh38.p13 chr1: 28,487,801-28,724,600 , GRCh37.p13 chr1: 28,814,313-29,051,112 SNORD99, PHACTR4, 15 more genes
    nsv4895641copy number variation1nstd200human GRCh38 chr1: 28,648,734-28,648,823 , GRCh37.p13 chr1: 28,975,246-28,975,335 RNU11, TAF12-DT, 1 more genes
    nsv4895640copy number variation1nstd200human GRCh38 chr1: 28,647,644-28,651,007 , GRCh37.p13 chr1: 28,974,156-28,977,519 TAF12, TAF12-DT, 1 more genes
    nsv4772833copy number variation1nstd200human GRCh37 chr1: 28,975,246-28,975,335 , GRCh38.p12 chr1: 28,648,734-28,648,823 RNU11, TAF12-DT, 1 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
    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
    nsv3907483copy number variation1nstd102humanPathogenic GRCh37 chr1: 27,289,536-32,744,646 , GRCh38 chr1: 26,963,045-32,279,045 , NCBI36 chr1: 27,162,123-32,517,233 ATP5IF1, LOC102723760, 138 more genes
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