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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978716inversion1nstd209human GRCh38 chr15: 44,871,104-45,015,879 , GRCh37.p13 chr15: 45,163,302-45,308,077 TERB2, SORD2P, 8 more genes
    nsv5935514copy number variation1nstd209human GRCh38 chr15: 44,963,725-44,963,785 , GRCh37.p13 chr15: 45,255,923-45,255,983 TERB2
    nsv5928657copy number variation1nstd209human GRCh38 chr15: 44,978,019-44,979,055 , GRCh37.p13 chr15: 45,270,217-45,271,253 TERB2
    nsv5865219copy number variation1nstd209human GRCh38 chr15: 44,965,948-44,969,373 , GRCh37.p13 chr15: 45,258,146-45,261,571 LOC100187725, TERB2
    nsv5863856copy number variation1nstd209human GRCh38 chr15: 44,944,892-44,958,579 , GRCh37.p13 chr15: 45,237,090-45,250,777 TERB2
    nsv5862789copy number variation1nstd209human GRCh38 chr15: 44,970,077-44,987,625 , GRCh37.p13 chr15: 45,262,275-45,279,823 TERB2, LOC100187725, 1 more genes
    nsv5862436copy number variation1nstd209human GRCh38 chr15: 44,956,025-44,964,895 , GRCh37.p13 chr15: 45,248,223-45,257,093 RNU6-1332P, TERB2
    nsv5859784copy number variation1nstd209human GRCh38 chr15: 44,970,296-44,972,322 , GRCh37.p13 chr15: 45,262,494-45,264,520 RNU6-966P, TERB2, 1 more genes
    nsv5851645copy number variation1nstd209human GRCh38 chr15: 44,969,574-44,973,365 , GRCh37.p13 chr15: 45,261,772-45,265,563 TERB2, LOC100187725, 1 more genes
    nsv5663518insertion1nstd207human GRCh38 chr15: 44,979,103-44,979,103 , GRCh37.p13 chr15: 45,271,301-45,271,301 TERB2
    nsv5660871insertion1nstd207human GRCh38 chr15: 44,970,883-44,970,883 , GRCh37.p13 chr15: 45,263,081-45,263,081 TERB2, LOC100187725
    nsv5655061insertion1nstd207human GRCh38 chr15: 44,975,659-44,975,659 , GRCh37.p13 chr15: 45,267,857-45,267,857 TERB2
    nsv5602151copy number variation1nstd207human GRCh38 chr15: 44,965,321-44,965,668 , GRCh37.p13 chr15: 45,257,519-45,257,866 TERB2
    nsv5599770copy number variation1nstd207human GRCh38 chr15: 44,962,171-44,962,487 , GRCh37.p13 chr15: 45,254,369-45,254,685 TERB2, RNU6-1332P
    nsv5590351copy number variation1nstd207human GRCh38 chr15: 44,971,767-44,974,921 , GRCh37.p13 chr15: 45,263,965-45,267,119 TERB2, LOC100187725, 1 more genes
    nsv5562309sequence alteration1nstd206human GRCh38 chr15: 44,859,031-45,026,043 , GRCh37.p13 chr15: 45,151,229-45,318,241 SORD, SORD2P, 9 more genes
    nsv5558579sequence alteration1nstd206human GRCh38 chr15: 44,876,360-45,010,315 , GRCh37.p13 chr15: 45,168,558-45,302,513 TERB2, LOC100187725, 8 more genes
    nsv5532238copy number variation1nstd206human GRCh38 chr15: 44,963,726-44,963,786 , GRCh37.p13 chr15: 45,255,924-45,255,984 TERB2
    nsv5518104copy number variation1nstd206human GRCh38 chr15: 44,917,155-45,003,000 , GRCh37.p13 chr15: 45,209,353-45,295,198 TERB2, LOC100129830, 6 more genes
    nsv5380762copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-45,898,712 , GRCh38.p12 chr15: 44,563,121-45,606,514 LOC100533853, RNU6-1108P, 44 more genes
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