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Items: 1 to 20 of 481

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045404inversion1nstd229human GRCh38 chr4: 158,555,779-158,560,701 , GRCh37.p13 chr4: 159,476,931-159,481,853 RXFP1
    nsv7039901inversion1nstd229human GRCh38 chr4: 158,555,629-158,564,458 , GRCh37.p13 chr4: 159,476,781-159,485,610 RXFP1
    nsv6754606copy number variation1nstd229human GRCh38 chr4: 158,641,901-158,645,600 , GRCh37.p13 chr4: 159,563,053-159,566,752 RXFP1
    nsv6754359copy number variation1nstd229human GRCh38 chr4: 158,526,201-158,554,000 , GRCh37.p13 chr4: 159,447,353-159,475,152 RXFP1
    nsv6753146copy number variation1nstd229human GRCh38 chr4: 158,518,318-158,528,759 , GRCh37.p13 chr4: 159,439,470-159,449,911 RXFP1
    nsv6751608copy number variation1nstd229human GRCh38 chr4: 158,530,801-158,544,300 , GRCh37.p13 chr4: 159,451,953-159,465,452 RXFP1
    nsv6751219copy number variation1nstd229human GRCh38 chr4: 158,595,177-158,597,518 , GRCh37.p13 chr4: 159,516,329-159,518,670 RXFP1
    nsv6749024copy number variation1nstd229human GRCh38 chr4: 158,641,467-158,650,942 , GRCh37.p13 chr4: 159,562,619-159,572,094 RXFP1
    nsv6748909copy number variation1nstd229human GRCh38 chr4: 158,641,801-158,651,500 , GRCh37.p13 chr4: 159,562,953-159,572,652 RXFP1
    nsv6746634copy number variation1nstd229human GRCh38 chr4: 158,631,036-158,635,778 , GRCh37.p13 chr4: 159,552,188-159,556,930 RXFP1
    nsv6745686copy number variation1nstd229human GRCh38 chr4: 158,564,975-158,568,518 , GRCh37.p13 chr4: 159,486,127-159,489,670 RXFP1
    nsv6744047copy number variation1nstd229human GRCh38 chr4: 158,648,390-158,656,755 , GRCh37.p13 chr4: 159,569,542-159,577,907 RXFP1
    nsv6742850copy number variation1nstd229human GRCh38 chr4: 158,640,552-158,728,570 , GRCh37.p13 chr4: 159,561,704-159,649,722 C4orf46, PPID, 2 more genes
    nsv6742049copy number variation1nstd229human GRCh38 chr4: 158,558,302-158,558,337 , GRCh37.p13 chr4: 159,479,454-159,479,489 RXFP1
    nsv6741624copy number variation1nstd229human GRCh38 chr4: 158,517,101-158,522,200 , GRCh37.p13 chr4: 159,438,253-159,443,352 RXFP1
    nsv6740611copy number variation1nstd229human GRCh38 chr4: 158,525,746-158,530,347 , GRCh37.p13 chr4: 159,446,898-159,451,499 RXFP1
    nsv6740038copy number variation1nstd229human GRCh38 chr4: 158,626,877-158,627,250 , GRCh37.p13 chr4: 159,548,029-159,548,402 RXFP1
    nsv6636412copy number variation1nstd102humanUncertain significance GRCh37 chr4: 158,682,606-159,762,612 , GRCh38.p12 chr4: 157,761,454-158,841,460 LOC105377509, GASK1B, 15 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6567266inversion1nstd223human GRCh38 chr4: 158,528,431-158,529,426 , GRCh37.p13 chr4: 159,449,583-159,450,578 RXFP1
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