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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5976461inversion1nstd209human GRCh38 chr2: 27,448,313-28,588,967 , GRCh37.p13 chr2: 27,671,180-28,811,834 , FOSL2, 31 more genes
    nsv4674305copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,387,514-29,616,031 , GRCh38.p12 chr2: 28,164,647-29,393,165 BABAM2, FOSL2, 27 more genes
    nsv4537769insertion1nstd166human GRCh37.p13 chr2: 28,530,688-28,530,688 , GRCh38.p12 chr2: 28,307,821-28,307,821 BABAM2, RPL23AP34, 1 more genes
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4318621inversion1nstd166human GRCh37.p13 chr2: 21,612,232-41,909,281 , GRCh38.p12 chr2: 21,389,360-41,682,141 , CAD, 329 more genes
    nsv3919769copy number variation1nstd102humanPathogenic NCBI36 chr2: 22,776,056-33,845,581 , GRCh37.p13 chr2: 22,922,551-33,992,077 , GRCh38.p12 chr2: 22,699,679-33,767,010 RNA5SP88, EIF2B4, 213 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 ALLC, LOC105373429, 674 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 LOC105373394, PGAM1P6, 507 more genes
    nsv3907033copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531 GTF3C2-AS1, LOC105373399, 434 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3890734copy number variation1nstd102humanPathogenic NCBI36 chr2: 22,656,029-28,601,557 , GRCh37 chr2: 22,802,524-28,748,053 , GRCh38 chr2: 22,579,652-28,525,186 MAPRE3-AS1, PPIL1P1, 142 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 3724 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 ATL2, UBXN2A, 465 more genes
    nsv3878768copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,306,106-30,052,309 , GRCh38.p12 chr2: 28,083,239-29,829,443 SNRPGP7, TRMT61B, 29 more genes
    nsv3877469copy number variation1nstd102humanPathogenic GRCh37 chr2: 28,069,882-43,543,420 , GRCh38.p12 chr2: 27,847,015-43,316,281 FOSL2, EIF2AK2, 219 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 RPL7P13, LINC01318, 426 more genes
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