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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979511insertion1nstd209human GRCh38 chr16: 23,510,928-23,510,928 , GRCh37.p13 chr16: 23,522,249-23,522,249 GGA2
    nsv5943085copy number variation1nstd209human GRCh38 chr16: 23,481,538-23,482,031 , GRCh37.p13 chr16: 23,492,859-23,493,352 GGA2
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5883790copy number variation1nstd209human GRCh38 chr16: 23,458,984-23,472,200 , GRCh37.p13 chr16: 23,470,305-23,483,521 GGA2
    nsv5590869copy number variation1nstd207human GRCh38 chr16: 23,462,701-23,462,910 , GRCh37.p13 chr16: 23,474,022-23,474,231 GGA2
    nsv5533855copy number variation1nstd206human GRCh38 chr16: 23,498,153-23,503,385 , GRCh37.p13 chr16: 23,509,474-23,514,706 CCNYL7, GGA2
    nsv5533425copy number variation1nstd206human GRCh38 chr16: 23,508,976-23,509,051 , GRCh37.p13 chr16: 23,520,297-23,520,372 GGA2
    nsv5390513copy number variation1nstd186human GRCh37 chr16: 23,474,146-23,474,333 , GRCh38.p12 chr16: 23,462,825-23,463,012 GGA2
    nsv5305759copy number variation1nstd204human GRCh38.p13 chr16: 23,462,805-23,463,090 , GRCh37.p13 chr16: 23,474,126-23,474,411 GGA2
    nsv5266082copy number variation1nstd204human GRCh38.p13 chr16: 23,390,301-23,477,900 , GRCh37.p13 chr16: 23,401,622-23,489,221 GGA2, RN7SKP23, 1 more genes
    nsv5153589mobile element insertion1nstd203human GRCh38 chr16: 23,498,436-23,498,447 , GRCh37.p13 chr16: 23,509,757-23,509,768 GGA2
    nsv5003198copy number variation1nstd200human GRCh38 chr16: 23,461,750-23,463,699 , GRCh37.p13 chr16: 23,473,071-23,475,020 GGA2
    nsv4994558copy number variation1nstd200human GRCh38 chr16: 23,496,226-23,496,906 , GRCh37.p13 chr16: 23,507,547-23,508,227 GGA2
    nsv4994556copy number variation1nstd200human GRCh38 chr16: 23,447,578-23,515,419 , GRCh37.p13 chr16: 23,458,899-23,526,740 GGA2, CCNYL7, 1 more genes
    nsv4864065copy number variation1nstd200human GRCh37 chr16: 23,470,370-23,483,667 , GRCh38.p12 chr16: 23,459,049-23,472,346 GGA2
    nsv4864063copy number variation1nstd200human GRCh37 chr16: 23,458,899-23,526,740 , GRCh38.p12 chr16: 23,447,578-23,515,419 CCNYL7, COG7, 1 more genes
    nsv4850739copy number variation1nstd200human GRCh37 chr16: 23,520,297-23,520,372 , GRCh38.p12 chr16: 23,508,976-23,509,051 GGA2
    nsv4850738copy number variation1nstd200human GRCh37 chr16: 23,492,859-23,493,321 , GRCh38.p12 chr16: 23,481,538-23,482,000 GGA2
    nsv4850737copy number variation1nstd200human GRCh37 chr16: 23,474,140-23,474,340 , GRCh38.p12 chr16: 23,462,819-23,463,019 GGA2
    nsv4735137copy number variation1nstd199human GRCh37 chr16: 23,474,127-23,474,336 , GRCh38.p12 chr16: 23,462,806-23,463,015 GGA2
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