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Items: 1 to 20 of 688

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961526insertion1nstd209human GRCh38 chr2: 171,033,547-171,033,547 , GRCh37.p13 chr2: 171,890,057-171,890,057 TLK1
    nsv5949182insertion1nstd209human GRCh38 chr2: 171,048,631-171,048,631 , GRCh37.p13 chr2: 171,905,141-171,905,141 TLK1
    nsv5906195copy number variation1nstd209human GRCh38 chr2: 171,177,085-171,177,394 , GRCh37.p13 chr2: 172,033,595-172,033,904 TLK1
    nsv5903677copy number variation1nstd209human GRCh38 chr2: 171,165,766-171,166,072 , GRCh37.p13 chr2: 172,022,276-172,022,582 TLK1
    nsv5898471copy number variation1nstd209human GRCh38 chr2: 171,072,731-171,076,180 , GRCh37.p13 chr2: 171,929,241-171,932,690 TLK1
    nsv5890750copy number variation1nstd209human GRCh38 chr2: 171,114,865-171,115,028 , GRCh37.p13 chr2: 171,971,375-171,971,538 TLK1
    nsv5888438copy number variation1nstd209human GRCh38 chr2: 171,086,861-171,086,985 , GRCh37.p13 chr2: 171,943,371-171,943,495 TLK1
    nsv5831434copy number variation1nstd209human GRCh38 chr2: 171,073,053-171,076,281 , GRCh37.p13 chr2: 171,929,563-171,932,791 TLK1
    nsv5692436mobile element insertion2nstd211human GRCh38 chr2: 171,033,564-171,033,564 , GRCh37.p13 chr2: 171,890,074-171,890,074 TLK1
    nsv5681258mobile element insertion1nstd211human GRCh38 chr2: 171,047,259-171,047,259 , GRCh37.p13 chr2: 171,903,769-171,903,769 TLK1
    nsv5680215mobile element insertion1nstd211human GRCh38 chr2: 171,094,573-171,094,573 , GRCh37.p13 chr2: 171,951,083-171,951,083 TLK1
    nsv5680143mobile element insertion1nstd211human GRCh38 chr2: 171,212,510-171,212,510 , GRCh37.p13 chr2: 172,069,020-172,069,020 TLK1
    nsv5618438insertion1nstd207human GRCh38 chr2: 171,033,547-171,033,547 , GRCh37.p13 chr2: 171,890,057-171,890,057 TLK1
    nsv5611651insertion1nstd207human GRCh38 chr2: 171,103,264-171,103,264 , GRCh37.p13 chr2: 171,959,774-171,959,774 TLK1
    nsv5611417insertion1nstd207human GRCh38 chr2: 171,048,630-171,048,630 , GRCh37.p13 chr2: 171,905,140-171,905,140 TLK1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5550566insertion1nstd206human GRCh38 chr2: 171,033,564-171,033,598 , GRCh37.p13 chr2: 171,890,074-171,890,108 TLK1
    nsv5542774insertion1nstd206human GRCh38 chr2: 171,048,660-171,048,677 , GRCh37.p13 chr2: 171,905,170-171,905,187 TLK1
    nsv5452874copy number variation1nstd206human GRCh38 chr2: 171,205,672-171,205,740 , GRCh37.p13 chr2: 172,062,182-172,062,250 TLK1
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