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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093395copy number variation1nstd102humanPathogenic GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323 TODL, MIR6074, 116 more genes
    nsv7077154inversion1nstd229human GRCh38 chr12: 69,110,254-73,283,220 , GRCh37.p13 chr12: 69,504,034-73,677,000 MYRFL, CNOT2, 46 more genes
    nsv7070040inversion1nstd229human GRCh38 chr12: 69,868,908-69,868,961 , GRCh37.p13 chr12: 70,262,688-70,262,741 MYRFL
    nsv7066132inversion1nstd229human GRCh38 chr12: 65,153,239-72,873,965 , GRCh37.p13 chr12: 65,547,019-73,267,745 IL26, RPL7P42, 119 more genes
    nsv7060197inversion1nstd229human GRCh38 chr12: 64,990,820-72,253,420 , GRCh37.p13 chr12: 65,384,600-72,647,200 LINC02384, LOC105369809, 122 more genes
    nsv6937264copy number variation1nstd229human GRCh38 chr12: 69,929,490-69,935,590 , GRCh37.p13 chr12: 70,323,270-70,329,370 MYRFL
    nsv6935461copy number variation1nstd229human GRCh38 chr12: 69,904,039-69,908,445 , GRCh37.p13 chr12: 70,297,819-70,302,225 MYRFL
    nsv6934592copy number variation1nstd229human GRCh38 chr12: 69,894,987-69,900,396 , GRCh37.p13 chr12: 70,288,767-70,294,176 MYRFL
    nsv6933839copy number variation1nstd229human GRCh38 chr12: 69,897,012-69,913,245 , GRCh37.p13 chr12: 70,290,792-70,307,025 MYRFL
    nsv6932684copy number variation1nstd229human GRCh38 chr12: 69,952,275-69,952,614 , GRCh37.p13 chr12: 70,346,055-70,346,394 MYRFL
    nsv6931220copy number variation1nstd229human GRCh38 chr12: 69,843,209-69,844,240 , GRCh37.p13 chr12: 70,236,989-70,238,020 MYRFL
    nsv6929620copy number variation1nstd229human GRCh38 chr12: 69,933,217-69,935,396 , GRCh37.p13 chr12: 70,326,997-70,329,176 MYRFL
    nsv6928151copy number variation1nstd229human GRCh38 chr12: 69,720,792-69,875,006 , GRCh37.p13 chr12: 70,114,572-70,268,786 MYRFL, RAB3IP, 1 more genes
    nsv6926217copy number variation1nstd229human GRCh38 chr12: 69,937,816-69,937,962 , GRCh37.p13 chr12: 70,331,596-70,331,742 MYRFL
    nsv6926015copy number variation1nstd229human GRCh38 chr12: 69,926,058-69,926,114 , GRCh37.p13 chr12: 70,319,838-70,319,894 MYRFL
    nsv6925075copy number variation1nstd229human GRCh38 chr12: 69,897,011-69,899,735 , GRCh37.p13 chr12: 70,290,791-70,293,515 MYRFL
    nsv6924359copy number variation1nstd229human GRCh38 chr12: 69,880,517-69,880,696 , GRCh37.p13 chr12: 70,274,297-70,274,476 MYRFL
    nsv6921648copy number variation1nstd229human GRCh38 chr12: 69,848,839-69,849,252 , GRCh37.p13 chr12: 70,242,619-70,243,032 MYRFL
    nsv6921428copy number variation1nstd229human GRCh38 chr12: 69,877,441-69,879,978 , GRCh37.p13 chr12: 70,271,221-70,273,758 MYRFL
    nsv6920892copy number variation1nstd229human GRCh38 chr12: 69,891,604-69,954,239 , GRCh37.p13 chr12: 70,285,384-70,348,019 MYRFL
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