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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953637insertion1nstd209human GRCh38 chr5: 137,975,980-137,975,980 , GRCh37.p13 chr5: 137,311,669-137,311,669 FAM13B
    nsv5892152copy number variation1nstd209human GRCh38 chr5: 137,976,273-137,977,721 , GRCh37.p13 chr5: 137,311,962-137,313,410 FAM13B
    nsv5841440copy number variation1nstd209human GRCh38 chr5: 137,976,234-137,977,482 , GRCh37.p13 chr5: 137,311,923-137,313,171 FAM13B
    nsv5728885mobile element insertion1nstd211human GRCh38 chr5: 138,023,869-138,023,869 , GRCh37.p13 chr5: 137,359,558-137,359,558 FAM13B
    nsv5725831mobile element insertion1nstd211human GRCh38 chr5: 138,030,664-138,030,664 , GRCh37.p13 chr5: 137,366,353-137,366,353 FAM13B
    nsv5724459mobile element insertion2nstd211human GRCh38 chr5: 137,974,663-137,974,663 , GRCh37.p13 chr5: 137,310,352-137,310,352 FAM13B
    nsv5690919mobile element insertion1nstd211human GRCh38 chr5: 138,007,822-138,007,822 , GRCh37.p13 chr5: 137,343,511-137,343,511 FAM13B
    nsv5687501mobile element insertion1nstd211human GRCh38 chr5: 137,966,566-137,966,566 , GRCh37.p13 chr5: 137,302,255-137,302,255 FAM13B
    nsv5682554mobile element insertion1nstd211human GRCh38 chr5: 138,012,238-138,012,238 , GRCh37.p13 chr5: 137,347,927-137,347,927 FAM13B
    nsv5629530insertion1nstd207human GRCh38 chr5: 137,983,213-137,983,213 , GRCh37.p13 chr5: 137,318,902-137,318,902 FAM13B
    nsv5562971mobile element insertion1nstd206human GRCh38 chr5: 137,974,677-137,974,714 , GRCh37.p13 chr5: 137,310,366-137,310,403 FAM13B
    nsv5562473mobile element insertion1nstd206human GRCh38 chr5: 138,030,664-138,030,715 , GRCh37.p13 chr5: 137,366,353-137,366,404 FAM13B
    nsv5561989mobile element insertion1nstd206human GRCh38 chr5: 138,023,869-138,023,920 , GRCh37.p13 chr5: 137,359,558-137,359,609 FAM13B
    nsv5473273copy number variation1nstd206human GRCh38 chr5: 138,046,987-138,049,556 , GRCh37.p13 chr5: 137,382,676-137,385,245 FAM13B
    nsv5471050copy number variation1nstd206human GRCh38 chr5: 137,856,777-138,124,570 , GRCh37.p13 chr5: 137,192,466-137,460,259 RNU6-460P, RNU6-1148P, 9 more genes
    nsv5463225copy number variation1nstd206human GRCh38 chr5: 137,987,257-137,987,315 , GRCh37.p13 chr5: 137,322,946-137,323,004 FAM13B
    nsv5461369copy number variation1nstd206human GRCh38 chr5: 138,028,983-138,032,411 , GRCh37.p13 chr5: 137,364,672-137,368,100 FAM13B-AS1, FAM13B
    nsv5460861copy number variation1nstd206human GRCh38 chr5: 137,976,286-137,977,784 , GRCh37.p13 chr5: 137,311,975-137,313,473 FAM13B
    nsv5401093mobile element insertion1nstd206human GRCh38 chr5: 138,007,822-138,007,873 , GRCh37.p13 chr5: 137,343,511-137,343,562 FAM13B
    nsv5381777copy number variation1nstd102humanPathogenic GRCh37 chr5: 136,409,875-137,739,167 , GRCh38.p12 chr5: 137,074,186-138,403,478 HNRNPA0, SPOCK1, 24 more genes
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