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Items: 1 to 20 of 182

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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
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5469543copy number variation1nstd206human GRCh38 chr4: 143,549,301-143,549,398 , GRCh37.p13 chr4: 144,470,454-144,470,551 SMARCA5
    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
    nsv4674499copy number variation1nstd102humanPathogenic GRCh37 chr4: 139,531,815-146,095,109 , GRCh38.p12 chr4: 138,610,661-145,173,957 GUSBP5, LOC100287014, 77 more genes
    nsv4540910insertion1nstd166human GRCh37.p13 chr4: 144,436,756-144,436,756 , GRCh38.p12 chr4: 143,515,603-143,515,603 SMARCA5
    nsv4455734copy number variation1nstd102humanUncertain significance GRCh37 chr4: 140,522,019-146,347,867 , GRCh38.p12 chr4: 139,600,865-145,426,715 RN7SL152P, MIR3139, 61 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
    nsv4372690copy number variation1nstd173human GRCh37 chr4: 144,422,010-144,443,350 , GRCh38.p12 chr4: 143,500,857-143,522,197 SMARCA5-AS1, SMARCA5
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4095761copy number variation1nstd166human GRCh37.p13 chr4: 144,470,454-144,470,551 , GRCh38.p12 chr4: 143,549,301-143,549,398 SMARCA5
    nsv3924487copy number variation1nstd102humanUncertain significance GRCh38 chr4: 143,139,072-143,763,698 , NCBI36 chr4: 144,279,675-144,904,301 , GRCh37 chr4: 144,060,225-144,684,851 GUSBP5, SMARCA5, 9 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
    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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