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Items: 1 to 20 of 141

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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
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv4873391inversion1nstd200human GRCh37 chr4: 137,941,721-143,237,901 , GRCh38.p12 chr4: 137,020,567-142,316,748 , MAML3, 68 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
    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
    nsv4456879copy number variation1nstd102humanUncertain significance GRCh37 chr4: 134,054,911-142,601,496 , GRCh38.p12 chr4: 133,133,756-141,680,343 NOCT, IL15, 81 more genes
    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
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4102968copy number variation1nstd166human GRCh37.p13 chr4: 142,185,800-142,500,162 , GRCh38.p12 chr4: 141,264,646-141,579,009 LINC02432, LINC02276
    nsv4096182copy number variation1nstd166human GRCh37.p13 chr4: 142,499,832-142,499,939 , GRCh38.p12 chr4: 141,578,679-141,578,786 LINC02276
    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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