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Items: 1 to 20 of 859

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119659copy number variation1nstd186human GRCh37 chr4: 141,841,365-141,844,287 , GRCh38.p12 chr4: 140,920,211-140,923,133 RNF150
    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
    nsv5954060insertion1nstd209human GRCh38 chr4: 140,997,688-140,997,688 , GRCh37.p13 chr4: 141,918,842-141,918,842 RNF150
    nsv5953573insertion1nstd209human GRCh38 chr4: 141,110,579-141,110,579 , GRCh37.p13 chr4: 142,031,733-142,031,733 RNF150
    nsv5904590copy number variation1nstd209human GRCh38 chr4: 140,895,858-140,896,730 , GRCh37.p13 chr4: 141,817,012-141,817,884 RNF150
    nsv5895911copy number variation1nstd209human GRCh38 chr4: 141,184,812-141,185,490 , GRCh37.p13 chr4: 142,105,966-142,106,644 RNF150
    nsv5892961copy number variation1nstd209human GRCh38 chr4: 140,927,691-140,928,158 , GRCh37.p13 chr4: 141,848,845-141,849,312 RNF150
    nsv5891316copy number variation1nstd209human GRCh38 chr4: 141,155,967-141,156,068 , GRCh37.p13 chr4: 142,077,121-142,077,222 RNF150
    nsv5889464copy number variation1nstd209human GRCh38 chr4: 141,005,774-141,006,086 , GRCh37.p13 chr4: 141,926,928-141,927,240 RNF150
    nsv5838000copy number variation2nstd209human GRCh38 chr4: 140,918,687-140,921,034 , GRCh37.p13 chr4: 141,839,841-141,842,188 RNF150
    nsv5729203mobile element insertion2nstd211human GRCh38 chr4: 141,179,296-141,179,296 , GRCh37.p13 chr4: 142,100,450-142,100,450 RNF150
    nsv5717353mobile element insertion2nstd211human GRCh38 chr4: 140,889,986-140,889,986 , GRCh37.p13 chr4: 141,811,140-141,811,140 RNF150
    nsv5715545mobile element insertion1nstd211human GRCh38 chr4: 141,169,586-141,169,586 , GRCh37.p13 chr4: 142,090,740-142,090,740 RNF150
    nsv5690758mobile element insertion1nstd211human GRCh38 chr4: 141,059,718-141,059,718 , GRCh37.p13 chr4: 141,980,872-141,980,872 RNF150
    nsv5680829mobile element insertion2nstd211human GRCh38 chr4: 141,167,495-141,167,495 , GRCh37.p13 chr4: 142,088,649-142,088,649 RNF150
    nsv5618892insertion1nstd207human GRCh38 chr4: 140,999,948-140,999,948 , GRCh37.p13 chr4: 141,921,102-141,921,102 RNF150
    nsv5613684insertion1nstd207human GRCh38 chr4: 141,155,967-141,155,967 , GRCh37.p13 chr4: 142,077,121-142,077,121 RNF150
    nsv5611375insertion1nstd207human GRCh38 chr4: 140,997,688-140,997,688 , GRCh37.p13 chr4: 141,918,842-141,918,842 RNF150
    nsv5610839insertion1nstd207human GRCh38 chr4: 141,110,579-141,110,579 , GRCh37.p13 chr4: 142,031,733-142,031,733 RNF150
    nsv5610460insertion1nstd207human GRCh38 chr4: 140,999,942-140,999,942 , GRCh37.p13 chr4: 141,921,096-141,921,096 RNF150
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