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Items: 1 to 20 of 132

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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
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5039478inversion1nstd200human GRCh38 chr4: 158,116,539-168,149,530 , GRCh37.p13 chr4: 159,037,691-169,070,681 MIR4454, LOC105377520, 93 more genes
    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
    nsv4674043copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318 CYP4V2, ZFP42, 319 more genes
    nsv4560349mobile element insertion1nstd166human GRCh37.p13 chr4: 166,325,286-166,325,286 , GRCh38.p12 chr4: 165,404,134-165,404,134 CPE, HADHAP1
    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
    nsv4457131copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,069,355-177,189,728 , GRCh38.p12 chr4: 164,148,203-176,268,577 LINC02269, NOL8P1, 140 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
    nsv4384387copy number variation1nstd173human GRCh37 chr4: 166,219,337-167,178,950 , GRCh38.p12 chr4: 165,298,185-166,257,798 LOC105377521, MSMO1, 13 more genes
    nsv4340612sequence alteration1nstd166human GRCh37.p13 chr4: 156,844,669-168,668,516 , GRCh38.p12 chr4: 155,923,517-167,747,365 , GK3, 107 more genes
    nsv3924394copy number variation1nstd102humanUncertain significance GRCh38 chr4: 164,837,643-167,576,305 , GRCh37 chr4: 165,758,795-168,497,456 , NCBI36 chr4: 165,978,245-168,734,031 LOC105377521, LOC391711, 34 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
    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
    nsv3919458copy number variation1nstd102humanPathogenic GRCh38 chr4: 155,162,982-170,959,553 , GRCh37 chr4: 156,084,134-171,880,704 , NCBI36 chr4: 156,303,584-172,117,279 AIDAP2, MTCYBP17, 172 more genes
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