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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5943708copy number variation1nstd209human GRCh38 chr19: 4,379,181-4,379,286 , GRCh37.p13 chr19: 4,379,178-4,379,283 SH3GL1
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5726513mobile element insertion1nstd211human GRCh38 chr19: 4,378,184-4,378,184 , GRCh37.p13 chr19: 4,378,181-4,378,181 SH3GL1
    nsv5723913mobile element insertion1nstd211human GRCh38 chr19: 4,378,196-4,378,196 , GRCh37.p13 chr19: 4,378,193-4,378,193 SH3GL1
    nsv5557764mobile element insertion1nstd206human GRCh38 chr19: 4,378,196-4,378,235 , GRCh37.p13 chr19: 4,378,193-4,378,232 SH3GL1
    nsv5518881copy number variation1nstd206human GRCh38 chr19: 4,396,869-4,397,121 , GRCh37.p13 chr19: 4,396,866-4,397,118 SH3GL1
    nsv5517762copy number variation1nstd206human GRCh38 chr19: 4,358,930-4,359,003 , GRCh37.p13 chr19: 4,358,927-4,359,000 MPND, SH3GL1
    nsv5299582copy number variation1nstd204human GRCh37.p13 chr19: 4,335,098-4,420,197 , GRCh38.p13 chr19: 4,335,101-4,420,200 , SH3GL1, 4 more genes
    nsv5298923copy number variation1nstd204human GRCh38.p13 chr19: 4,375,876-4,383,199 , GRCh37.p13 chr19: 4,375,873-4,383,196 SH3GL1
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5288993copy number variation1nstd204human GRCh38.p13 chr19: 4,398,548-4,402,093 , GRCh37.p13 chr19: 4,398,545-4,402,090 CHAF1A, SH3GL1
    nsv5284500copy number variation1nstd204human GRCh38.p13 chr19: 4,068,001-4,541,200 , GRCh37.p13 chr19: 4,067,999-4,541,212 , EIF1P6, 20 more genes
    nsv5212573mobile element deletion1nstd204human GRCh38.p13 chr19: 4,382,228-4,382,582 , GRCh37.p13 chr19: 4,382,225-4,382,579 SH3GL1
    nsv5179403mobile element insertion1nstd203human GRCh38 chr19: 4,371,976-4,371,993 , GRCh37.p13 chr19: 4,371,973-4,371,990 SH3GL1
    nsv5027327copy number variation1nstd200human GRCh38 chr19: 4,362,482-4,362,593 , GRCh37.p13 chr19: 4,362,479-4,362,590 SH3GL1
    nsv4769716mobile element deletion1nstd200human GRCh37 chr19: 4,382,251-4,382,554 , GRCh38.p12 chr19: 4,382,254-4,382,557 SH3GL1
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4652040copy number variation1nstd186human GRCh37 chr19: 4,399,000-4,404,575 , GRCh38.p12 chr19: 4,399,003-4,404,578 SH3GL1, CHAF1A
    nsv4547517insertion1nstd166human GRCh37.p13 chr19: 4,358,927-4,358,927 , GRCh38.p12 chr19: 4,358,930-4,358,930 SH3GL1, MPND
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