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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969430inversion1nstd209human GRCh38 chr10: 24,952,189-24,957,813 , GRCh37.p13 chr10: 25,241,118-25,246,742 PRTFDC1, THNSL1
    nsv5915684copy number variation1nstd209human GRCh38 chr10: 24,952,238-24,963,959 , GRCh37.p13 chr10: 25,241,167-25,252,888 THNSL1, PRTFDC1
    nsv5865820copy number variation1nstd209human GRCh38 chr10: 24,952,160-24,959,874 , GRCh37.p13 chr10: 25,241,089-25,248,803 THNSL1, PRTFDC1
    nsv5694655mobile element insertion1nstd211human GRCh38 chr10: 24,956,360-24,956,360 , GRCh37.p13 chr10: 25,245,289-25,245,289 THNSL1
    nsv5477503copy number variation1nstd206human GRCh38 chr10: 24,976,559-24,976,616 , GRCh37.p13 chr10: 25,265,488-25,265,545 THNSL1
    nsv5408130mobile element insertion1nstd206human GRCh38 chr10: 24,956,360-24,956,400 , GRCh37.p13 chr10: 25,245,289-25,245,329 THNSL1
    nsv5137855mobile element insertion1nstd203human GRCh38 chr10: 24,972,191-24,972,207 , GRCh37.p13 chr10: 25,261,120-25,261,136 THNSL1
    nsv4975462copy number variation1nstd200human GRCh38 chr10: 24,969,109-24,980,941 , GRCh37.p13 chr10: 25,258,038-25,269,870 ENKUR, THNSL1
    nsv4975461copy number variation1nstd200human GRCh38 chr10: 24,960,629-24,960,880 , GRCh37.p13 chr10: 25,249,558-25,249,809 THNSL1
    nsv4975460copy number variation1nstd200human GRCh38 chr10: 24,947,681-24,954,028 , GRCh37.p13 chr10: 25,236,610-25,242,957 PRTFDC1, THNSL1
    nsv4735959copy number variation1nstd199human GRCh37 chr10: 25,277,591-25,277,643 , GRCh38.p12 chr10: 24,988,662-24,988,714 THNSL1, ENKUR
    nsv4617300copy number variation1nstd183human GRCh37 chr10: 25,260,466-25,268,199 , GRCh38.p12 chr10: 24,971,537-24,979,270 THNSL1
    nsv4553602insertion1nstd166human GRCh37.p13 chr10: 25,261,120-25,261,120 , GRCh38.p12 chr10: 24,972,191-24,972,191 THNSL1
    nsv4491367mobile element insertion1nstd166human GRCh37.p13 chr10: 25,245,274-25,245,274 , GRCh38.p12 chr10: 24,956,345-24,956,345 THNSL1
    nsv4481150mobile element insertion1nstd166human GRCh37.p13 chr10: 25,251,043-25,251,043 , GRCh38.p12 chr10: 24,962,114-24,962,114 THNSL1
    nsv4455901copy number variation1nstd102humanUncertain significance GRCh37 chr10: 25,133,682-25,277,446 , GRCh38.p12 chr10: 24,844,753-24,988,517 THNSL1, ENKUR, 2 more genes
    nsv4418398copy number variation1nstd174human GRCh37 chr10: 25,277,423-25,277,846 , GRCh38.p12 chr10: 24,988,494-24,988,917 ENKUR, THNSL1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4182275copy number variation1nstd166human GRCh37.p13 chr10: 25,304,162-25,307,763 , GRCh38.p12 chr10: 25,015,233-25,018,834 THNSL1, ENKUR
    nsv4173908copy number variation1nstd166human GRCh37.p13 chr10: 25,258,069-25,269,841 , GRCh38.p12 chr10: 24,969,140-24,980,912 THNSL1, ENKUR
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