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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130801insertion1nstd186human GRCh37 chr13: 79,946,950-79,946,953 , GRCh38.p12 chr13: 79,372,815-79,372,818 RBM26
    nsv5976455insertion1nstd209human GRCh38 chr13: 79,373,377-79,373,377 , GRCh37.p13 chr13: 79,947,512-79,947,512 RBM26
    nsv5972548insertion1nstd209human GRCh38 chr13: 79,372,794-79,372,794 , GRCh37.p13 chr13: 79,946,929-79,946,929 RBM26
    nsv5970242insertion1nstd209human GRCh38 chr13: 79,319,949-79,319,949 , GRCh37.p13 chr13: 79,894,084-79,894,084 RBM26
    nsv5938935copy number variation1nstd209human GRCh38 chr13: 79,392,110-79,392,181 , GRCh37.p13 chr13: 79,966,245-79,966,316 RBM26
    nsv5932186copy number variation1nstd209human GRCh38 chr13: 77,934,881-83,910,012 , GRCh37.p13 chr13: 78,509,016-84,484,147 NDFIP2, LINC01068, 54 more genes
    nsv5928621copy number variation1nstd209human GRCh38 chr13: 79,372,870-79,373,028 , GRCh37.p13 chr13: 79,947,005-79,947,163 RBM26
    nsv5661556insertion1nstd207human GRCh38 chr13: 79,373,367-79,373,367 , GRCh37.p13 chr13: 79,947,502-79,947,502 RBM26
    nsv5650734insertion1nstd207human GRCh38 chr13: 79,392,113-79,392,113 , GRCh37.p13 chr13: 79,966,248-79,966,248 RBM26
    nsv5601648copy number variation1nstd207human GRCh38 chr13: 79,373,490-79,373,544 , GRCh37.p13 chr13: 79,947,625-79,947,679 RBM26
    nsv5598917copy number variation1nstd207human GRCh38 chr13: 79,372,873-79,372,986 , GRCh37.p13 chr13: 79,947,008-79,947,121 RBM26
    nsv5598043copy number variation1nstd207human GRCh38 chr13: 79,392,110-79,392,181 , GRCh37.p13 chr13: 79,966,245-79,966,316 RBM26
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5552149insertion1nstd206human GRCh38 chr13: 79,372,815-79,372,818 , GRCh37.p13 chr13: 79,946,950-79,946,953 RBM26
    nsv5512366copy number variation1nstd206human GRCh38 chr13: 79,308,663-79,310,051 , GRCh37.p13 chr13: 79,882,798-79,884,186 RBM26
    nsv5509476copy number variation1nstd206human GRCh38 chr13: 79,401,607-79,401,664 , GRCh37.p13 chr13: 79,975,742-79,975,799 RBM26
    nsv5508395copy number variation1nstd206human GRCh38 chr13: 79,392,202-79,392,297 , GRCh37.p13 chr13: 79,966,337-79,966,432 RBM26
    nsv5505571copy number variation1nstd206human GRCh38 chr13: 79,375,086-79,375,162 , GRCh37.p13 chr13: 79,949,221-79,949,297 RBM26
    nsv5504804copy number variation1nstd206human GRCh38 chr13: 79,331,728-79,333,281 , GRCh37.p13 chr13: 79,905,863-79,907,416 RBM26
    nsv5497751copy number variation1nstd206human GRCh38 chr13: 79,362,402-79,362,459 , GRCh37.p13 chr13: 79,936,537-79,936,594 RBM26
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