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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899231copy number variation1nstd209human GRCh38 chr2: 216,144,112-216,144,265 , GRCh37.p13 chr2: 217,008,835-217,008,988 XRCC5
    nsv5724812mobile element insertion1nstd211human GRCh38 chr2: 216,144,940-216,144,940 , GRCh37.p13 chr2: 217,009,663-217,009,663 XRCC5
    nsv5689952mobile element insertion1nstd211human GRCh38 chr2: 216,122,619-216,122,619 , GRCh37.p13 chr2: 216,987,342-216,987,342 XRCC5
    nsv5683638mobile element insertion1nstd211human GRCh38 chr2: 216,120,172-216,120,172 , GRCh37.p13 chr2: 216,984,895-216,984,895 XRCC5
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452910copy number variation1nstd206human GRCh38 chr2: 216,184,291-216,184,517 , GRCh37.p13 chr2: 217,049,014-217,049,240 XRCC5
    nsv5451215copy number variation1nstd206human GRCh38 chr2: 216,139,461-216,140,662 , GRCh37.p13 chr2: 217,004,184-217,005,385 XRCC5
    nsv5449842copy number variation1nstd206human GRCh38 chr2: 216,146,400-216,146,453 , GRCh37.p13 chr2: 217,011,123-217,011,176 XRCC5
    nsv5447228copy number variation1nstd206human GRCh38 chr2: 216,196,525-216,199,452 , GRCh37.p13 chr2: 217,061,248-217,064,175 XRCC5
    nsv5438303copy number variation1nstd206human GRCh38 chr2: 216,160,531-216,160,622 , GRCh37.p13 chr2: 217,025,254-217,025,345 XRCC5
    nsv5410229mobile element insertion1nstd206human GRCh38 chr2: 216,120,172-216,120,223 , GRCh37.p13 chr2: 216,984,895-216,984,946 XRCC5
    nsv5395391mobile element insertion1nstd206human GRCh38 chr2: 216,122,619-216,122,670 , GRCh37.p13 chr2: 216,987,342-216,987,393 XRCC5
    nsv5029880inversion1nstd200human GRCh38 chr2: 213,444,845-219,177,092 , GRCh37.p13 chr2: 214,309,569-220,041,814 , LOC102724861, 122 more genes
    nsv4916813copy number variation1nstd200human GRCh38 chr2: 216,196,525-216,199,452 , GRCh37.p13 chr2: 217,061,248-217,064,175 XRCC5
    nsv4916812copy number variation1nstd200human GRCh38 chr2: 216,177,959-216,182,875 , GRCh37.p13 chr2: 217,042,682-217,047,598 XRCC5
    nsv4916811copy number variation1nstd200human GRCh38 chr2: 216,176,213-216,176,288 , GRCh37.p13 chr2: 217,040,936-217,041,011 LOC100421349, XRCC5
    nsv4916810copy number variation1nstd200human GRCh38 chr2: 216,163,740-216,166,605 , GRCh37.p13 chr2: 217,028,463-217,031,328 XRCC5
    nsv4795927copy number variation1nstd200human GRCh37 chr2: 217,042,682-217,047,598 , GRCh38.p12 chr2: 216,177,959-216,182,875 XRCC5
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728446copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 215,122,019-220,397,907 , GRCh38.p12 chr2: 214,257,295-219,533,185 AAMP, ATIC, 139 more genes
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