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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137192copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,520,701-234,168,331 , GRCh38.p12 chr2: 231,655,990-233,259,685 NEU2, MIR562, 38 more genes
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv6697757copy number variation1nstd229human GRCh38 chr2: 232,376,701-232,410,300 , GRCh37.p13 chr2: 233,241,411-233,275,010 ALPG, ECEL1P2, 1 more genes
    nsv6696773copy number variation1nstd229human GRCh38 chr2: 232,346,582-232,453,118 , GRCh37.p13 chr2: 233,211,292-233,317,828 ALPP, ECEL1P3, 4 more genes
    nsv6695237copy number variation1nstd229human GRCh38 chr2: 232,362,328-232,544,996 , GRCh37.p13 chr2: 233,227,038-233,409,706 ALPG, CHRND, 9 more genes
    nsv6692763copy number variation1nstd229human GRCh38 chr2: 232,361,901-232,757,800 , GRCh37.p13 chr2: 233,226,611-233,622,510 LOC105373929, CHRND, 16 more genes
    nsv6690553copy number variation1nstd229human GRCh38 chr2: 232,293,780-232,529,812 , GRCh37.p13 chr2: 233,158,490-233,394,522 ECEL1P1, DIS3L2, 10 more genes
    nsv6689075copy number variation1nstd229human GRCh38 chr2: 232,388,792-232,455,618 , GRCh37.p13 chr2: 233,253,502-233,320,328 DIS3L2P1, ECEL1P1, 2 more genes
    nsv6688989copy number variation1nstd229human GRCh38 chr2: 232,273,801-232,522,100 , GRCh37.p13 chr2: 233,138,511-233,386,810 PRSS56, ECEL1P2, 9 more genes
    nsv6685264copy number variation1nstd229human GRCh38 chr2: 232,368,188-232,411,914 , GRCh37.p13 chr2: 233,232,898-233,276,624 ECEL1P2, ALPP, 1 more genes
    nsv6682306copy number variation1nstd229human GRCh38 chr2: 232,162,461-232,514,393 , GRCh37.p13 chr2: 233,027,171-233,379,103 ECEL1P2, ECEL1P1, 9 more genes
    nsv6628066copy number variation3nstd224human GRCh37 chr2: 233,215,403-233,310,149 , GRCh38.p12 chr2: 232,350,693-232,445,439 ALPP, ALPG, 4 more genes
    nsv6628014copy number variation1nstd224human GRCh37 chr2: 233,204,359-233,321,379 , GRCh38.p12 chr2: 232,339,649-232,456,669 ALPI, ALPP, 7 more genes
    nsv6628013copy number variation1nstd224human GRCh37 chr2: 233,204,359-233,321,089 , GRCh38.p12 chr2: 232,339,649-232,456,379 ALPI, ALPP, 7 more genes
    nsv6628012copy number variation1nstd224human GRCh37 chr2: 233,200,512-233,311,947 , GRCh38.p12 chr2: 232,335,802-232,447,237 ALPP, ALPG, 6 more genes
    nsv6628011copy number variation1nstd224human GRCh37 chr2: 233,200,512-233,302,141 , GRCh38.p12 chr2: 232,335,802-232,437,431 ALPP, ALPG, 5 more genes
    nsv6628010copy number variation1nstd224human GRCh37 chr2: 233,198,664-233,321,379 , GRCh38.p12 chr2: 232,333,954-232,456,669 ALPI, ALPP, 7 more genes
    nsv6627641copy number variation2nstd224human GRCh37 chr2: 233,215,403-233,315,499 , GRCh38.p12 chr2: 232,350,693-232,450,789 ALPP, ALPG, 4 more genes
    nsv6627640copy number variation1nstd224human GRCh37 chr2: 233,215,403-233,300,816 , GRCh38.p12 chr2: 232,350,693-232,436,106 ALPP, ECEL1P1, 3 more genes
    nsv6627565copy number variation3nstd224human GRCh37 chr2: 233,215,403-233,321,379 , GRCh38.p12 chr2: 232,350,693-232,456,669 ALPI, ALPP, 5 more genes
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