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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933059copy number variation1nstd209human GRCh38 chr12: 102,082,035-102,082,197 , GRCh37.p13 chr12: 102,475,813-102,475,975 NUP37
    nsv5714456mobile element insertion2nstd211human GRCh38 chr12: 102,085,991-102,085,991 , GRCh37.p13 chr12: 102,479,769-102,479,769 NUP37
    nsv5708974mobile element insertion2nstd211human GRCh38 chr12: 102,082,477-102,082,477 , GRCh37.p13 chr12: 102,476,255-102,476,255 NUP37
    nsv5556088mobile element insertion1nstd206human GRCh38 chr12: 102,086,004-102,086,042 , GRCh37.p13 chr12: 102,479,782-102,479,820 NUP37
    nsv5511941copy number variation1nstd206human GRCh38 chr12: 102,081,211-102,081,386 , GRCh37.p13 chr12: 102,474,989-102,475,164 NUP37
    nsv5426553mobile element insertion1nstd206human GRCh38 chr12: 102,082,477-102,082,528 , GRCh37.p13 chr12: 102,476,255-102,476,306 NUP37
    nsv5309022copy number variation1nstd204human GRCh38.p13 chr12: 102,085,569-102,086,223 , GRCh37.p13 chr12: 102,479,347-102,480,001 NUP37
    nsv5261560copy number variation1nstd204human GRCh38.p13 chr12: 102,091,601-102,096,100 , GRCh37.p13 chr12: 102,485,379-102,489,878 NUP37
    nsv5199152mobile element insertion1nstd203human GRCh38 chr12: 102,085,991-102,085,991 , GRCh37.p13 chr12: 102,479,769-102,479,769 NUP37
    nsv5181173mobile element insertion1nstd203human GRCh38 chr12: 102,082,681-102,082,681 , GRCh37.p13 chr12: 102,476,459-102,476,459 NUP37
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995325copy number variation1nstd200human GRCh38 chr12: 102,085,577-102,086,216 , GRCh37.p13 chr12: 102,479,355-102,479,994 NUP37
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4842174copy number variation1nstd200human GRCh37 chr12: 102,479,355-102,479,994 , GRCh38.p12 chr12: 102,085,577-102,086,216 NUP37
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4680088copy number variation1nstd189human GRCh37.p13 chr12: 102,055,253-102,714,201 , GRCh38.p12 chr12: 101,661,475-102,320,423 MYBPC1, PMCH, 21 more genes
    nsv4675271copy number variation1nstd102humanUncertain significance GRCh37 chr12: 101,953,283-102,683,945 , GRCh38.p12 chr12: 101,559,505-102,290,167 DRAM1, RNU6-172P, 23 more genes
    nsv4576761mobile element insertion1nstd166human GRCh37.p13 chr12: 102,479,769-102,479,769 , GRCh38.p12 chr12: 102,085,991-102,085,991 NUP37
    nsv4576331mobile element insertion1nstd166human GRCh37.p13 chr12: 102,476,442-102,476,442 , GRCh38.p12 chr12: 102,082,664-102,082,664 NUP37
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