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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138994copy number variation1nstd232human GRCh37.p13 chr2: 242,749,084-242,749,157 , GRCh38.p12 chr2: 241,808,001-241,808,074 , GRCh38.p12 chr2|NT_187527.1: 20,099-20,172 NEU4
    nsv7138169copy number variation1nstd232human GRCh37.p13 chr2: 242,756,591-242,756,719 , GRCh38.p12 chr2|NT_187527.1: 27,367-27,491 NEU4
    nsv7050262inversion1nstd229human GRCh38 chr2: 241,804,298-241,814,694 , GRCh37.p13 chr2: 242,743,713-242,755,891 NEU4, GAL3ST2
    nsv7047138inversion1nstd229human GRCh38 chr2: 241,752,746-241,987,074 , GRCh37.p13 chr2: 242,692,161-242,929,225 LINC01238, RTP5, 9 more genes
    nsv6717538copy number variation1nstd229human GRCh38 chr2: 241,801,948-242,059,511 , GRCh37.p13 chr2: 242,741,363-243,001,662 LOC107986004, LINC01880, 11 more genes
    nsv6715509copy number variation1nstd229human GRCh38 chr2: 241,779,697-241,813,067 , GRCh37.p13 chr2: 242,719,112-242,754,205 GAL3ST2, NEU4
    nsv6713067copy number variation1nstd229human GRCh38 chr2: 241,777,521-241,834,240 , GRCh37.p13 chr2: 242,716,936-242,776,417 GAL3ST2, NEU4, 1 more genes
    nsv6711989copy number variation1nstd229human GRCh38 chr2: 241,731,561-241,908,453 , GRCh37.p13 chr2: 242,670,976-242,850,604 GAL3ST2, PDCD1, 8 more genes
    nsv6711074copy number variation1nstd229human GRCh38 chr2: 241,812,962-241,817,008 , GRCh37.p13 chr2: 242,754,100-242,758,334 LOC107986004, NEU4
    nsv6711026copy number variation1nstd229human GRCh38 chr2: 241,788,179-241,843,942 , GRCh37.p13 chr2: 242,727,594-242,786,094 LOC107986004, NEU4, 1 more genes
    nsv6707329copy number variation1nstd229human GRCh38 chr2: 241,709,883-241,892,927 , GRCh37.p13 chr2: 242,649,298-242,835,078 D2HGDH, LINC01237, 9 more genes
    nsv6704553copy number variation1nstd229human GRCh38 chr2: 241,801,160-241,863,459 , GRCh37.p13 chr2: 242,740,575-242,805,611 GAL3ST2, LOC107986004, 3 more genes
    nsv6704155copy number variation1nstd229human GRCh38 chr2: 241,771,426-241,833,880 , GRCh37.p13 chr2: 242,710,841-242,776,057 NEU4, LOC107986004, 1 more genes
    nsv6702834copy number variation1nstd229human GRCh38 chr2: 241,795,001-242,003,800 , GRCh37.p13 chr2: 242,734,416-242,945,951 GAL3ST2, LOC105373978, 9 more genes
    nsv6702092copy number variation1nstd229human GRCh38 chr2: 241,812,969-241,817,008 , GRCh37.p13 chr2: 242,754,107-242,758,334 NEU4, LOC107986004
    nsv6698745copy number variation1nstd229human GRCh38 chr2: 241,795,701-241,911,700 , GRCh37.p13 chr2: 242,735,116-242,853,851 GAL3ST2, NEU4, 7 more genes
    nsv6636841copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,878,509-242,783,384 , GRCh38.p12 chr2: 235,969,865-241,841,232 COPS8-DT, MTND5P46, 128 more genes
    nsv6636733copy number variation1nstd102humanUncertain significance GRCh37 chr2: 242,379,032-242,783,384 , GRCh38.p12 chr2: 241,439,617-241,841,232 ATG4B, THAP4, 15 more genes
    nsv6636673copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,942,616-242,783,384 , GRCh38.p12 chr2: 235,033,972-241,841,232 LINC02991, OR6B3, 136 more genes
    nsv6636482copy number variation1nstd102humanUncertain significance GRCh37 chr2: 242,533,423-242,783,384 , GRCh38.p12 chr2: 241,594,008-241,841,232 D2HGDH, NEU4, 6 more genes
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