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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6689752copy number variation1nstd229human GRCh38 chr2: 158,756,909-158,821,470 , GRCh37.p13 chr2: 159,613,421-159,677,982 DAPL1
    nsv6689513copy number variation1nstd229human GRCh38 chr2: 158,805,484-158,806,363 , GRCh37.p13 chr2: 159,661,996-159,662,875 DAPL1
    nsv6688927copy number variation1nstd229human GRCh38 chr2: 158,619,485-159,171,773 , GRCh37.p13 chr2: 159,475,997-160,028,284 BTF3L4P2, DAPL1, 10 more genes
    nsv6686899copy number variation1nstd229human GRCh38 chr2: 158,790,463-159,097,019 , GRCh37.p13 chr2: 159,646,975-159,953,531 GSTM3P2, TANC1, 8 more genes
    nsv6684579copy number variation1nstd229human GRCh38 chr2: 158,800,292-158,808,199 , GRCh37.p13 chr2: 159,656,804-159,664,711 DAPL1
    nsv6682686copy number variation1nstd229human GRCh38 chr2: 158,805,501-158,806,300 , GRCh37.p13 chr2: 159,662,013-159,662,812 DAPL1
    nsv6680288copy number variation1nstd229human GRCh38 chr2: 158,805,370-158,806,361 , GRCh37.p13 chr2: 159,661,882-159,662,873 DAPL1
    nsv6636277copy number variation1nstd102humanUncertain significance GRCh37 chr2: 159,214,954-160,334,904 , GRCh38.p12 chr2: 158,358,442-159,478,393 WDSUB1, BAZ2B, 20 more genes
    nsv6545821inversion1nstd223human GRCh38 chr2: 158,806,674-158,807,826 , GRCh37.p13 chr2: 159,663,186-159,664,338 DAPL1
    nsv6350178copy number variation1nstd223human GRCh38 chr2: 158,805,482-158,806,360 , GRCh37.p13 chr2: 159,661,994-159,662,872 DAPL1
    nsv6343878copy number variation1nstd223human GRCh38 chr2: 158,790,463-159,097,019 , GRCh37.p13 chr2: 159,646,975-159,953,531 DAPL1, GSTM3P2, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313568copy number variation1nstd102humanPathogenic GRCh37 chr2: 158,950,827-164,456,735 , GRCh38.p12 chr2: 158,094,315-163,600,225 PSMD14-DT, DPP4, 70 more genes
    nsv6300467copy number variation1nstd186human GRCh37 chr2: 159,646,975-159,953,533 , GRCh38.p12 chr2: 158,790,463-159,097,021 RNU6-580P, OR7E28P, 8 more genes
    nsv6291262copy number variation1nstd102humannot provided GRCh37 chr2: 152,967,964-160,089,210 , GRCh38.p12 chr2: 152,111,450-159,232,699 GALNT13-AS1, ARL6IP6, 85 more genes
    nsv6283541insertion1nstd214human GRCh38 chr2: 158,805,484-158,805,484 , GRCh37.p13 chr2: 159,661,996-159,661,996 DAPL1
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv5986484copy number variation1nstd212human GRCh38 chr2: 158,805,482-158,806,360 , GRCh37.p13 chr2: 159,661,994-159,662,872 DAPL1
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