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Items: 1 to 20 of 2097

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126261insertion1nstd186human GRCh37 chr2: 137,968,934-137,968,957 , GRCh38.p12 chr2: 137,211,364-137,211,387 THSD7B
    nsv6125178insertion1nstd186human GRCh37 chr2: 138,033,775-138,033,812 , GRCh38.p12 chr2: 137,276,205-137,276,242 THSD7B
    nsv5973870inversion1nstd209human GRCh38 chr2: 137,055,293-137,056,524 , GRCh37.p13 chr2: 137,812,863-137,814,094 THSD7B
    nsv5964717insertion1nstd209human GRCh38 chr2: 137,607,171-137,607,171 , GRCh37.p13 chr2: 138,364,741-138,364,741 THSD7B
    nsv5964479insertion1nstd209human GRCh38 chr2: 137,276,191-137,276,191 , GRCh37.p13 chr2: 138,033,761-138,033,761 THSD7B
    nsv5960706insertion1nstd209human GRCh38 chr2: 137,502,222-137,502,222 , GRCh37.p13 chr2: 138,259,792-138,259,792 THSD7B, LOC105373634
    nsv5960059insertion1nstd209human GRCh38 chr2: 137,419,378-137,419,378 , GRCh37.p13 chr2: 138,176,948-138,176,948 THSD7B
    nsv5959446insertion1nstd209human GRCh38 chr2: 137,590,792-137,590,792 , GRCh37.p13 chr2: 138,348,362-138,348,362 THSD7B
    nsv5955709insertion1nstd209human GRCh38 chr2: 137,303,657-137,303,657 , GRCh37.p13 chr2: 138,061,227-138,061,227 THSD7B
    nsv5952532insertion1nstd209human GRCh38 chr2: 137,462,776-137,462,776 , GRCh37.p13 chr2: 138,220,346-138,220,346 THSD7B
    nsv5949145insertion1nstd209human GRCh38 chr2: 137,211,336-137,211,336 , GRCh37.p13 chr2: 137,968,906-137,968,906 THSD7B
    nsv5948268insertion1nstd209human GRCh38 chr2: 136,769,582-136,769,582 , GRCh37.p13 chr2: 137,527,152-137,527,152 THSD7B
    nsv5903552copy number variation1nstd209human GRCh38 chr2: 137,331,117-137,331,194 , GRCh37.p13 chr2: 138,088,687-138,088,764 THSD7B
    nsv5903440copy number variation1nstd209human GRCh38 chr2: 137,286,575-137,286,735 , GRCh37.p13 chr2: 138,044,145-138,044,305 THSD7B
    nsv5902941copy number variation1nstd209human GRCh38 chr2: 137,003,736-137,061,871 , GRCh37.p13 chr2: 137,761,306-137,819,441 THSD7B
    nsv5902820copy number variation1nstd209human GRCh38 chr2: 137,331,150-137,331,346 , GRCh37.p13 chr2: 138,088,720-138,088,916 THSD7B
    nsv5900226copy number variation1nstd209human GRCh38 chr2: 137,487,718-137,488,061 , GRCh37.p13 chr2: 138,245,288-138,245,631 THSD7B
    nsv5899915copy number variation1nstd209human GRCh38 chr2: 137,044,157-137,049,599 , GRCh37.p13 chr2: 137,801,727-137,807,169 THSD7B
    nsv5893923copy number variation1nstd209human GRCh38 chr2: 137,225,734-137,226,888 , GRCh37.p13 chr2: 137,983,304-137,984,458 THSD7B
    nsv5891952copy number variation1nstd209human GRCh38 chr2: 137,161,042-137,165,544 , GRCh37.p13 chr2: 137,918,612-137,923,114 THSD7B
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