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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934164copy number variation1nstd209human GRCh38 chr12: 98,605,575-98,605,711 , GRCh37.p13 chr12: 98,999,353-98,999,489 SLC25A3
    nsv5695061mobile element insertion2nstd211human GRCh38 chr12: 98,606,550-98,606,550 , GRCh37.p13 chr12: 99,000,328-99,000,328 SLC25A3
    nsv5661173insertion1nstd207human GRCh38 chr12: 98,606,536-98,606,536 , GRCh37.p13 chr12: 99,000,314-99,000,314 SLC25A3
    nsv5420102mobile element insertion1nstd206human GRCh38 chr12: 98,606,550-98,606,601 , GRCh37.p13 chr12: 99,000,328-99,000,379 SLC25A3
    nsv5379791translocation1nstd200human GRCh38 chr12: 98,605,303-98,605,303 , GRCh38 chr12: 98,606,424-98,606,424 , GRCh37.p13 chr12: 98,999,081-98,999,081 , GRCh37.p13 chr12: 99,000,202-99,000,202 SLC25A3
    nsv5356304translocation1nstd200human GRCh38 chr12: 98,605,299-98,605,299 , GRCh38 chr12: 98,606,202-98,606,202 , GRCh37.p13 chr12: 98,999,077-98,999,077 , GRCh37.p13 chr12: 98,999,980-98,999,980 SLC25A3
    nsv5335194translocation1nstd200human GRCh37 chr12: 98,999,980-98,999,980 , GRCh37 chr12: 98,999,077-98,999,077 , GRCh38.p12 chr12: 98,606,202-98,606,202 , GRCh38.p12 chr12: 98,605,299-98,605,299 SLC25A3
    nsv5128021mobile element insertion1nstd203human GRCh38 chr12: 98,595,279-98,595,298 , GRCh37.p13 chr12: 98,989,057-98,989,076 SLC25A3
    nsv5121863mobile element insertion1nstd203human GRCh38 chr12: 98,606,536-98,606,546 , GRCh37.p13 chr12: 99,000,314-99,000,324 SLC25A3
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    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
    nsv4607129copy number variation1nstd183human GRCh37 chr12: 98,977,196-98,985,625 , GRCh38.p12 chr12: 98,583,418-98,591,847 SLC25A3, PPIAP8
    nsv4511703mobile element insertion1nstd166human GRCh37.p13 chr12: 98,988,717-98,988,717 , GRCh38.p12 chr12: 98,594,939-98,594,939 SLC25A3
    nsv4455620copy number variation1nstd102humanUncertain significance GRCh37 chr12: 98,360,850-99,487,172 , GRCh38.p12 chr12: 97,967,072-99,093,394 LOC105369933, ANKS1B, 17 more genes
    nsv4455472copy number variation1nstd102humanUncertain significance GRCh37 chr12: 98,968,226-99,077,328 , GRCh38.p12 chr12: 98,574,448-98,683,550 IKBIP, SNORA53, 3 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4230843copy number variation1nstd166human GRCh37.p13 chr12: 98,932,298-99,049,729 , GRCh38.p12 chr12: 98,538,520-98,655,951 APAF1, SLC25A3, 4 more genes
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