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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116994copy number variation25nstd145human GRCh37 chr16: 55,799,053-55,821,304 , GRCh38.p12 chr16: 55,765,141-55,787,392 CES1P1
    nsv3117460copy number variation3nstd145human GRCh37 chr3: 41,615,210-41,634,835 , GRCh38.p12 chr3: 41,573,719-41,593,344 ULK4
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3117920copy number variation33nstd145human GRCh37 chr17: 50,117,130-50,126,228 , GRCh38.p12 chr17: 52,039,770-52,048,868 CA10
    nsv3117545copy number variation9nstd145human GRCh37 chrX: 29,600,070-29,608,901 , GRCh38.p12 chrX: 29,581,953-29,590,784 IL1RAPL1
    nsv3112409copy number variation2nstd145human GRCh37 chr12: 4,864,846-4,872,424 , GRCh38.p12 chr12: 4,755,680-4,763,258 GALNT8
    nsv3110514copy number variation75nstd145human GRCh37 chr8: 51,031,100-51,038,303 , GRCh38.p12 chr8: 50,118,540-50,125,743 SNTG1
    nsv3112901copy number variation1nstd145human GRCh37 chr6: 147,222,001-147,228,187 , GRCh38.p12 chr6: 146,900,865-146,907,051 STXBP5-AS1
    nsv3116197copy number variation63nstd145human GRCh37 chr7: 151,606-157,474 , GRCh38.p12 chr7: 151,606-157,474 , GRCh38.p12 chr7|NT_187558.1: 107,411-113,280 , GRCh38.p12 chr7|NT_187653.1: 143,927-149,795 LINC03014
    nsv3115596copy number variation45nstd145human GRCh37 chr3: 148,964,056-148,969,130 , GRCh38.p12 chr3: 149,246,269-149,251,343 CPHL1P
    nsv3113139copy number variation39nstd145human GRCh37 chr13: 32,533,792-32,538,481 , GRCh38.p12 chr13: 31,959,655-31,964,344 EEF1DP3
    nsv3117774copy number variation53nstd145human GRCh37 chr1: 174,796,674-174,801,029 , GRCh38.p12 chr1: 174,827,536-174,831,891 RABGAP1L
    nsv3117206copy number variation28nstd145human GRCh37 chr4: 138,095,710-138,099,949 , GRCh38.p12 chr4: 137,174,556-137,178,795 LINC02511
    nsv3111978copy number variation21nstd145human GRCh37 chr13: 79,203,351-79,207,511 , GRCh38.p12 chr13: 78,629,216-78,633,376 OBI1
    nsv3112046copy number variation55nstd145human GRCh37 chr19: 54,556,015-54,560,055 , GRCh38.p12 chr19: 54,052,761-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571061.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571057.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571058.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571059.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571060.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571056.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571055.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571054.1: 27,128-31,168 VSTM1
    nsv3110470copy number variation26nstd145human GRCh37 chr1: 106,018,381-106,022,354 , GRCh38.p12 chr1: 105,475,759-105,479,732 LOC105378881
    nsv3112736copy number variation1nstd145human GRCh37 chr19: 28,802,340-28,806,132 , GRCh38.p12 chr19: 28,311,433-28,315,225
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3111613copy number variation17nstd145human GRCh37 chr5: 151,514,653-151,518,262 , GRCh38.p12 chr5: 152,135,092-152,138,701 LINC01933
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