U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 97

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv482890sequence alteration1nstd40human NCBI34 chr15: 24,350,621-24,538,325 , GRCh37.p13 chr15: 26,803,260-26,990,964 , GRCh38.p12 chr15: 26,558,113-26,745,817 GABRB3
    nsv482262sequence alteration2nstd40human NCBI34 chr12: 33,629,831-33,813,501 , GRCh37.p13 chr12: 33,738,564-33,922,234 , GRCh38.p12 chr12: 33,585,629-33,769,299 LOC105369726
    nsv482724sequence alteration1nstd40human NCBI34 chr6: 57,444,281-57,620,889 , GRCh37.p13 chr6: 57,397,445-57,574,053 , GRCh38.p12 chr6: 60,429,700-60,606,306 PRIM2BP
    nsv482503sequence alteration1nstd40human NCBI34 chrX: 87,423,675-87,593,692 , GRCh37.p13 chrX: 88,651,818-88,821,835 , GRCh38.p12 chrX: 89,396,819-89,566,836 LOC102724150
    nsv482575sequence alteration1nstd40human NCBI34 chr7: 66,289,930-66,447,957 , GRCh37.p13 chr7: 66,878,314-67,036,341 , GRCh38.p12 chr7: 67,413,327-67,571,354 LOC105375340
    nsv482683sequence alteration3nstd40human NCBI34 chrX: 61,099,673-61,202,320 , GRCh37.p13 chrX|NW_004070881.1: 29,145-131,792 , GRCh37.p13 chrX: 62,232,882-62,335,529 , GRCh38.p12 chrX: 63,013,412-63,116,059 LOC100533729
    nsv482672sequence alteration2nstd40human NCBI34 chr2: 97,307,990-97,456,304 , GRCh37.p13 chr2: 97,823,234-97,920,629 , GRCh38.p12 chr2: 97,157,497-97,254,892 ANKRD36
    nsv482353sequence alteration1nstd40human NCBI34 chr15: 29,602,056-29,690,456 , GRCh37.p13 chr15: 31,886,000-31,974,400 , GRCh38.p12 chr15: 31,593,797-31,682,197 , GRCh38.p12 chr15|NT_187660.1: 3,878,947-3,967,345 , GRCh38.p12 chr15|NW_011332701.1: 3,766,495-3,854,893 OTUD7A
    nsv482481sequence alteration1nstd40human NCBI34 chr9: 225,831-420,014 , GRCh37.p13 chr9: 235,831-430,014 , GRCh38.p12 chr9: 235,831-430,014 DOCK8, LOC105375945
    nsv482900sequence alteration1nstd40human NCBI34 chr17: 411,080-598,333 , GRCh37.p13 chr17: 426,330-613,583 , GRCh38.p12 chr17: 523,090-710,343 , GRCh38.p12 chr17|NW_017363817.1: 82,567-269,820 VPS53, RPS4XP17
    nsv482343sequence alteration1nstd40human NCBI34 chr1: 22,551,497-22,732,885 , GRCh37.p13 chr1: 23,082,022-23,263,410 , GRCh38.p12 chr1: 22,755,529-22,936,917 EPHB2, MIR4253
    nsv482886sequence alteration20nstd40human NCBI34 chr8: 332,250-511,073 , GRCh37.p13 chr8: 342,250-521,073 , GRCh38.p12 chr8: 392,250-571,073 FBXO25, TDRP
    nsv482255sequence alteration1nstd40human NCBI34 chr11: 21,521,156-21,689,467 , GRCh37.p13 chr11: 21,556,847-21,725,158 , GRCh38.p12 chr11: 21,535,301-21,703,612 NELL1,
    nsv482263sequence alteration1nstd40human NCBI34 chr2: 144,825,328-144,976,047 , GRCh37.p13 chr2: 144,614,559-144,765,278 , GRCh38.p12 chr2: 143,856,990-144,007,711 GTDC1, LOC101928386
    nsv482710sequence alteration1nstd40human NCBI34 chr7: 71,472,438-71,622,982 , GRCh37.p13 chr7|NW_003871064.1: 124,600-260,683 , GRCh37.p13 chr7: 72,060,321-72,196,404 , GRCh38.p12 chr7: 72,595,336-72,745,892 TYW1B, MIR4650-2
    nsv482730sequence alteration1nstd40human NCBI34 chr2: 151,130,045-151,279,465 , GRCh37.p13 chr2: 150,927,500-151,076,920 , GRCh38.p12 chr2: 150,070,986-150,220,406 LOC105373682, LINC01818
    nsv482253sequence alteration2nstd40human NCBI34 chr9: 65,619,734-65,841,058 , GRCh38.p12 chr9: 64,476,875-64,698,199 , GRCh37.p13 chr9: 69,489,293-69,710,617 AQP7P2, CNN2P3, 3 more genes
    nsv482798sequence alteration1nstd40human NCBI34 chr1: 142,602,658-142,811,865 , GRCh38.p12 chr1: 148,825,338-149,034,607 , GRCh37.p13 chr1: 144,849,836-145,057,046 PDE4DIP, RN7SKP88, 2 more genes
    nsv482670sequence alteration2nstd40human NCBI34 chr7: 6,880,129-7,076,587 , GRCh37.p13 chr7: 7,135,792-7,332,250 , GRCh38.p12 chr7: 7,096,161-7,292,619 C1GALT1, LOC100131257, 2 more genes
    nsv482379sequence alteration1nstd40human NCBI34 chr11: 47,611,824-47,801,481 , GRCh37.p13 chr11: 47,647,515-47,837,172 , GRCh38.p12 chr11: 47,625,963-47,815,620 , GRCh38.p12 chr11|NW_019805496.1: 53,787-247,987 NUP160, FNBP4, 3 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center