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Items: 1 to 20 of 1397

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127129insertion1nstd186human GRCh37 chr6: 5,315,949-5,315,954 , GRCh38.p12 chr6: 5,315,716-5,315,721 FARS2
    nsv5972256inversion1nstd209human GRCh38 chr6: 5,767,255-5,767,497 , GRCh37.p13 chr6: 5,767,488-5,767,730 FARS2
    nsv5964442insertion1nstd209human GRCh38 chr6: 5,539,381-5,539,381 , GRCh37.p13 chr6: 5,539,614-5,539,614 FARS2
    nsv5962417insertion1nstd209human GRCh38 chr6: 5,315,738-5,315,738 , GRCh37.p13 chr6: 5,315,971-5,315,971 FARS2
    nsv5961870insertion1nstd209human GRCh38 chr6: 5,341,226-5,341,226 , GRCh37.p13 chr6: 5,341,459-5,341,459 FARS2
    nsv5960911insertion1nstd209human GRCh38 chr6: 5,407,066-5,407,066 , GRCh37.p13 chr6: 5,407,299-5,407,299 FARS2
    nsv5959353insertion1nstd209human GRCh38 chr6: 5,717,937-5,717,937 , GRCh37.p13 chr6: 5,718,170-5,718,170 FARS2
    nsv5958492insertion1nstd209human GRCh38 chr6: 5,348,527-5,348,527 , GRCh37.p13 chr6: 5,348,760-5,348,760 FARS2
    nsv5956321insertion1nstd209human GRCh38 chr6: 5,333,158-5,333,158 , GRCh37.p13 chr6: 5,333,391-5,333,391 FARS2
    nsv5953587insertion1nstd209human GRCh38 chr6: 5,488,639-5,488,639 , GRCh37.p13 chr6: 5,488,872-5,488,872 FARS2
    nsv5951622insertion1nstd209human GRCh38 chr6: 5,584,108-5,584,108 , GRCh37.p13 chr6: 5,584,341-5,584,341 FARS2
    nsv5950223insertion1nstd209human GRCh38 chr6: 5,525,242-5,525,242 , GRCh37.p13 chr6: 5,525,475-5,525,475 FARS2
    nsv5905894copy number variation1nstd209human GRCh38 chr6: 5,537,455-5,537,594 , GRCh37.p13 chr6: 5,537,688-5,537,827 FARS2
    nsv5901776copy number variation1nstd209human GRCh38 chr6: 5,728,237-5,729,701 , GRCh37.p13 chr6: 5,728,470-5,729,934 FARS2
    nsv5901416copy number variation1nstd209human GRCh38 chr6: 5,705,312-5,710,558 , GRCh37.p13 chr6: 5,705,545-5,710,791 FARS2
    nsv5898360copy number variation1nstd209human GRCh38 chr6: 5,661,776-5,661,856 , GRCh37.p13 chr6: 5,662,009-5,662,089 FARS2
    nsv5897759copy number variation1nstd209human GRCh38 chr6: 5,624,092-5,624,175 , GRCh37.p13 chr6: 5,624,325-5,624,408 FARS2
    nsv5897646copy number variation1nstd209human GRCh38 chr6: 5,539,456-5,546,473 , GRCh37.p13 chr6: 5,539,689-5,546,706 FARS2
    nsv5892224copy number variation1nstd209human GRCh38 chr6: 5,435,442-5,441,424 , GRCh37.p13 chr6: 5,435,675-5,441,657 FARS2
    nsv5891247copy number variation1nstd209human GRCh38 chr6: 5,606,338-5,609,854 , GRCh37.p13 chr6: 5,606,571-5,610,087 FARS2, HNRNPA1P37
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