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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5223784copy number variation1nstd204human GRCh38.p13 chr4: 154,562,001-154,565,300 , GRCh37.p13 chr4: 155,483,153-155,486,452 FGB
    nsv4929761copy number variation1nstd200human GRCh38 chr4: 154,567,671-154,567,897 , GRCh37.p13 chr4: 155,488,823-155,489,049 FGB
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4674602copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 153,061,243-157,994,448 , GRCh38.p12 chr4: 152,140,091-157,073,296 ANXA2P1, CTSO, 84 more genes
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4456414copy number variation1nstd102humanUncertain significance GRCh37 chr4: 154,907,679-159,012,980 , GRCh38.p12 chr4: 153,986,527-158,091,828 LOC105377508, MAP9-AS1, 59 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 more genes
    nsv4388052copy number variation1nstd173human GRCh37 chr4: 155,369,485-155,673,906 , GRCh38.p12 chr4: 154,448,333-154,752,754 FGB, PLRG1, 8 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv3955666copy number variation1nstd168human GRCh38 chr4: 154,517,492-154,568,163 , GRCh37.p13 chr4: 155,438,644-155,489,315 RNU6-1285P, FGB, 3 more genes
    nsv3924008copy number variation1nstd102humanPathogenic GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788 PPID, METTL14-DT, 828 more genes
    nsv3923416copy number variation1nstd102humanPathogenic GRCh37 chr4: 154,577,937-155,849,925 , NCBI36 chr4: 154,797,387-156,069,375 , GRCh38 chr4: 153,656,785-154,928,773 TLR2, RNU2-44P, 20 more genes
    nsv3922745copy number variation1nstd102humanPathogenic NCBI36 chr4: 139,651,136-191,121,344 , GRCh37 chr4: 139,431,686-190,828,225 , GRCh38 chr4: 138,510,532-189,963,195 TMEM131L, MTCO1P9, 622 more genes
    nsv3918110copy number variation1nstd102humanPathogenic NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225 SCRG1, KRT18P51, 770 more genes
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