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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141375insertion1nstd232human GRCh37.p13 chr2: 13,502,783-13,502,783 , GRCh38.p12 chr2: 13,362,658-13,362,658 LOC105373437
    nsv7139833insertion1nstd232human GRCh37.p13 chr2: 13,502,111-13,502,111 , GRCh38.p12 chr2: 13,361,986-13,361,986 LOC105373437
    nsv7042112inversion1nstd229human GRCh38 chr2: 13,292,334-13,362,168 , GRCh37.p13 chr2: 13,432,459-13,502,293 LOC105373437, LOC105373436
    nsv6677391copy number variation1nstd229human GRCh38 chr2: 12,795,776-13,413,500 , GRCh37.p13 chr2: 12,935,902-13,553,625 LOC105373484, LOC105373437, 2 more genes
    nsv6676068copy number variation1nstd229human GRCh38 chr2: 13,336,701-13,365,000 , GRCh37.p13 chr2: 13,476,826-13,505,125 LOC105373437
    nsv6675168copy number variation1nstd229human GRCh38 chr2: 13,391,844-13,401,182 , GRCh37.p13 chr2: 13,531,969-13,541,307 LOC105373437
    nsv6674177copy number variation1nstd229human GRCh38 chr2: 13,362,901-13,376,500 , GRCh37.p13 chr2: 13,503,026-13,516,625 LOC105373437
    nsv6666617copy number variation1nstd229human GRCh38 chr2: 13,335,540-13,562,177 , GRCh37.p13 chr2: 13,475,665-13,702,302 LOC105373485, LOC105373437
    nsv6663651copy number variation1nstd229human GRCh38 chr2: 13,071,890-13,378,670 , GRCh37.p13 chr2: 13,212,015-13,518,795 LOC105373436, LOC105373437, 1 more genes
    nsv6659921copy number variation1nstd229human GRCh38 chr2: 13,392,752-13,409,076 , GRCh37.p13 chr2: 13,532,877-13,549,201 LOC105373437
    nsv6658627copy number variation1nstd229human GRCh38 chr2: 13,363,310-13,363,452 , GRCh37.p13 chr2: 13,503,435-13,503,577 LOC105373437
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6627699copy number variation1nstd224human GRCh37 chr2: 13,536,772-14,330,209 , GRCh38.p12 chr2: 13,396,647-14,190,084 LOC105373437, LOC105373485, 3 more genes
    nsv6627690copy number variation1nstd224human GRCh37 chr2: 13,204,511-14,330,209 , GRCh38.p12 chr2: 13,064,386-14,190,084 NACAP9, LOC105373436, 5 more genes
    nsv6627257copy number variation1nstd224human GRCh37 chr2: 13,536,772-14,366,696 , GRCh38.p12 chr2: 13,396,647-14,226,572 NACAP9, LOC107985854, 3 more genes
    nsv6627256copy number variation4nstd224human GRCh37 chr2: 13,536,772-14,335,308 , GRCh38.p12 chr2: 13,396,647-14,195,184 LOC105373437, LOC105373438, 3 more genes
    nsv6540066inversion1nstd223human GRCh38 chr2: 13,362,845-13,485,429 , GRCh37.p13 chr2: 13,502,970-13,625,554 LOC105373437
    nsv6353855copy number variation1nstd223human GRCh38 chr2: 13,392,901-13,408,800 , GRCh37.p13 chr2: 13,533,026-13,548,925 LOC105373437
    nsv6351661copy number variation1nstd223human GRCh38 chr2: 13,393,801-13,394,700 , GRCh37.p13 chr2: 13,533,926-13,534,825 LOC105373437
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