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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5868766copy number variation1nstd209human GRCh38 chr1: 151,069,897-151,070,171 , GRCh37.p13 chr1: 151,042,373-151,042,647 MLLT11, GABPB2
    nsv5724252mobile element insertion1nstd211human GRCh38 chr1: 151,064,385-151,064,385 , GRCh37.p13 chr1: 151,036,861-151,036,861 MLLT11
    nsv5560892mobile element insertion1nstd206human GRCh38 chr1: 151,064,385-151,064,436 , GRCh37.p13 chr1: 151,036,861-151,036,912 MLLT11
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5212609copy number variation1nstd204human GRCh38.p13 chr1: 151,052,501-151,062,000 , GRCh37.p13 chr1: 151,024,977-151,034,476 MLLT11, CDC42SE1
    nsv4903854copy number variation1nstd200human GRCh38 chr1: 151,067,563-151,067,746 , GRCh37.p13 chr1: 151,040,039-151,040,222 MLLT11
    nsv4903853copy number variation1nstd200human GRCh38 chr1: 151,061,412-151,064,086 , GRCh37.p13 chr1: 151,033,888-151,036,562 MLLT11
    nsv4781178copy number variation1nstd200human GRCh37 chr1: 151,042,090-151,042,247 , GRCh38.p12 chr1: 151,069,614-151,069,771 GABPB2, MLLT11
    nsv4781177copy number variation1nstd200human GRCh37 chr1: 151,033,888-151,036,562 , GRCh38.p12 chr1: 151,061,412-151,064,086 MLLT11
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4712598copy number variation1nstd195human GRCh37 chr1: 151,042,151-151,571,701 , GRCh38.p12 chr1: 151,069,675-151,599,225 PI4KB, PSMD4, 24 more genes
    nsv4705049copy number variation1nstd195human GRCh37 chr1: 150,824,351-151,042,101 , GRCh38.p12 chr1: 150,851,875-151,069,625 ARNT, ANXA9, 15 more genes
    nsv4568582mobile element insertion1nstd166human GRCh37.p13 chr1: 151,036,844-151,036,844 , GRCh38.p12 chr1: 151,064,368-151,064,368 MLLT11
    nsv4068737copy number variation1nstd166human GRCh37.p13 chr1: 151,039,659-151,039,785 , GRCh38.p12 chr1: 151,067,183-151,067,309 MLLT11
    nsv4056985copy number variation1nstd166human GRCh37.p13 chr1: 151,029,927-151,039,379 , GRCh38.p12 chr1: 151,057,451-151,066,903 CDC42SE1, MLLT11
    nsv3962701copy number variation1nstd168human GRCh38 chr1: 151,000,704-151,111,850 , GRCh37.p13 chr1: 150,973,180-151,084,326 MLLT11, C1orf56, 7 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
    nsv3907566copy number variation1nstd102humanLikely pathogenic NCBI36 chr1: 149,228,433-149,823,877 , GRCh37 chr1: 150,961,809-151,557,253 , GRCh38 chr1: 150,989,333-151,584,777 PI4KB, PSMB4, 31 more genes
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