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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
    nsv4935896copy number variation1nstd200human GRCh38 chr4: 131,472,882-132,279,221 , GRCh37.p13 chr4: 132,394,037-133,200,376 , RPL7AP28, 5 more genes
    nsv4935894copy number variation1nstd200human GRCh38 chr4: 131,396,084-131,559,955 , GRCh37.p13 chr4: 132,317,239-132,481,110 LINC02377
    nsv4792247copy number variation1nstd200human GRCh37 chr4: 132,317,239-132,481,110 , GRCh38.p12 chr4: 131,396,084-131,559,955 LINC02377
    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
    nsv4673997copy number variation1nstd102humanUncertain significance GRCh37 chr4: 128,898,820-132,769,588 , GRCh38.p12 chr4: 127,977,665-131,848,433 RNU6-224P, LOC100128983, 29 more genes
    nsv4587368copy number variation1nstd183human GRCh37 chr4: 132,444,190-132,456,924 , GRCh38.p12 chr4: 131,523,035-131,535,769 LINC02377
    nsv4587317copy number variation1nstd183human GRCh37 chr4: 132,437,915-132,456,924 , GRCh38.p12 chr4: 131,516,760-131,535,769 LINC02377
    nsv4472951mobile element insertion1nstd166human GRCh37.p13 chr4: 132,445,086-132,445,086 , GRCh38.p12 chr4: 131,523,931-131,523,931 LINC02377
    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
    nsv3962084copy number variation1nstd168human GRCh38 chr4: 131,503,305-131,589,614 , GRCh37.p13 chr4: 132,424,460-132,510,769 LINC02377
    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
    nsv3923773copy number variation1nstd102humanUncertain significance GRCh37 chr4: 132,266,740-132,906,467 , NCBI36 chr4: 132,486,190-133,125,917 , GRCh38 chr4: 131,345,585-131,985,312 RN7SL205P, SNHG27, 3 more genes
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