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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116250copy number variation1nstd186human GRCh37 chr19: 88,000-200,000 , GRCh38.p12 chr19: 88,000-200,000 OR4G3P, OR4G1P, 6 more genes
    nsv5415550copy number variation1nstd206human GRCh38 chr19: 88,000-200,000 , GRCh37.p13 chr19: 88,000-200,000 OR4G3P, OR4G1P, 6 more genes
    nsv5294480copy number variation1nstd204human GRCh38.p13 chr19: 158,101-204,900 , GRCh37.p13 chr19: 158,101-204,900 CICP19, SEPTIN14P19, 2 more genes
    nsv5294081copy number variation1nstd204human GRCh38.p13 chr19: 179,101-206,900 , GRCh37.p13 chr19: 179,101-206,900 CICP19, SEPTIN14P19, 2 more genes
    nsv4667421copy number variation2nstd186human GRCh37 chr19: 70,342-201,929 , GRCh38.p12 chr19: 70,342-201,929 LOC105376912, LINC01002, 10 more genes
    nsv4641804copy number variation5nstd186human GRCh37 chr19: 162,000-187,000 , GRCh38.p12 chr19: 162,000-187,000 SEPTIN14P19
    nsv4625565copy number variation2nstd183human GRCh37 chr19: 70,342-201,929 , GRCh38.p12 chr19: 70,342-201,929 MIR1302-11, OR4G3P, 10 more genes
    nsv4623834copy number variation1nstd183human GRCh37 chr19: 172,370-200,977 , GRCh38.p12 chr19: 172,370-200,977 CICP19, LINC01002, 1 more genes
    nsv4622213copy number variation1nstd183human GRCh37 chr19: 60,110-243,066 , GRCh38.p12 chr19: 60,110-243,066 LOC107985295, CICP19, 14 more genes
    nsv4420172copy number variation1nstd174human GRCh37 chr19: 60,002-305,459 , GRCh38.p12 chr19: 60,002-305,459 PLPP2, MIER2, 17 more genes
    nsv4418860copy number variation1nstd174human GRCh37 chr19: 190,564-265,805 , GRCh38.p12 chr19: 190,564-265,805 LINC01002, CICP19, 5 more genes
    nsv4042377copy number variation9nstd166human GRCh37.p13 chr19: 162,000-187,000 , GRCh38.p12 chr19: 162,000-187,000 SEPTIN14P19
    nsv3962882copy number variation1nstd168human GRCh38 chr19: 79,701-208,249 , GRCh37.p13 chr19: 79,701-208,249 OR4G3P, OR4G1P, 7 more genes
    nsv3921979copy number variation1nstd102humanBenign NCBI36 chr19: 42,171-153,952 , GRCh37 chr19: 91,171-202,952 , GRCh38 chr19: 91,171-202,952 OR4F17, OR4F8P, 7 more genes
    nsv3917219copy number variation1nstd102humanBenign GRCh37 chr19: 61,112-202,952 , NCBI36 chr19: 12,112-153,952 , GRCh38 chr19: 61,112-202,952 WBP1LP11, WASH5P, 11 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3890380copy number variation1nstd102humanBenign GRCh37 chr19: 189,846-234,224 , GRCh38.p12 chr19: 189,846-234,224 LINC01002, CICP19, 4 more genes
    nsv3371848copy number variation9nstd162human GRCh38 chr19: 68,801-199,700 , GRCh37.p13 chr19: 68,801-199,700 OR4G3P, OR4G1P, 10 more genes
    nsv3358056copy number variation4nstd162human GRCh38 chr19: 170,201-195,300 , GRCh37.p13 chr19: 170,201-195,300 LINC01002, CICP19, 1 more genes
    nsv3344494copy number variation4nstd162human GRCh38 chr19: 167,301-217,800 , GRCh37.p13 chr19: 167,301-217,800 LINC01002, CICP19, 2 more genes
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