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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3888005copy number variation1nstd102humanBenign GRCh37 chr1: 16,367,339-16,382,003 , GRCh38.p12 chr1: 16,040,844-16,055,508 CLCNKB
    nsv3874925copy number variation1nstd102humanBenign GRCh37 chr1: 16,367,339-16,380,582 , GRCh38.p12 chr1: 16,040,844-16,054,087 CLCNKB
    nsv3879477copy number variation1nstd102humanBenign GRCh37 chr1: 16,372,151-16,381,893 , GRCh38.p12 chr1: 16,045,656-16,055,398 CLCNKB
    nsv3884673copy number variation1nstd102humanBenign GRCh37 chr1: 16,368,324-16,377,108 , GRCh38.p12 chr1: 16,041,829-16,050,613 CLCNKB
    nsv4685629copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,372,179-16,388,605 , GRCh38.p12 chr1: 16,045,684-16,062,110 CLCNKB, FAM131C
    nsv6112678copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,370,960-16,383,841 , GRCh38.p12 chr1: 16,044,465-16,057,346 CLCNKB, FAM131C
    nsv7098712copy number variation1nstd102humanPathogenic GRCh38 chr1: 16,044,452-16,056,956 , GRCh37.p13 chr1: 16,370,947-16,383,451 CLCNKB, FAM131C
    nsv3884721copy number variation2nstd102humanBenign GRCh37 chr1: 16,367,339-16,382,966 , GRCh38.p12 chr1: 16,040,844-16,056,471 CLCNKB, FAM131C
    nsv3890309copy number variation1nstd102humanBenign GRCh37 chr1: 16,364,253-16,376,855 , GRCh38 chr1: 16,037,758-16,050,360 , NCBI36 chr1: 16,236,840-16,249,442 CLCNKB, FAM131C2P
    nsv3884570copy number variation2nstd102humanBenign GRCh37 chr1: 16,372,151-16,384,554 , GRCh38.p12 chr1: 16,045,656-16,058,059 CLCNKB, FAM131C
    nsv3876007copy number variation1nstd102humanBenign GRCh37 chr1: 16,367,339-16,389,026 , GRCh38.p12 chr1: 16,040,844-16,062,531 CLCNKB, FAM131C
    nsv3876896copy number variation1nstd102humanBenign GRCh37 chr1: 16,372,151-16,390,104 , GRCh38.p12 chr1: 16,045,656-16,063,609 CLCNKB, FAM131C
    nsv3885141copy number variation1nstd102humanBenign GRCh37 chr1: 16,367,339-16,384,499 , GRCh38.p12 chr1: 16,040,844-16,058,004 CLCNKB, FAM131C
    nsv3880500copy number variation1nstd102humanBenign GRCh37 chr1: 16,370,314-16,383,267 , GRCh38.p12 chr1: 16,043,819-16,056,772 CLCNKB, FAM131C
    nsv7093131copy number variation1nstd102humanPathogenic GRCh38 chr1: 16,034,051-16,043,881 , GRCh37.p13 chr1: 16,360,546-16,370,376 CLCNKB, CLCNKA, 1 more genes
    nsv3888586copy number variation1nstd102humanBenign GRCh37 chr1: 16,358,248-16,382,966 , GRCh38.p12 chr1: 16,031,753-16,056,471 CLCNKB, FAM131C, 2 more genes
    nsv3877795copy number variation1nstd102humanBenign GRCh37 chr1: 16,352,547-16,370,851 , GRCh38.p12 chr1: 16,026,052-16,044,356 CLCNKB, CLCNKA, 1 more genes
    nsv3877891copy number variation1nstd102humanBenign GRCh37 chr1: 16,360,487-16,368,324 , GRCh38.p12 chr1: 16,033,992-16,041,829 CLCNKB, FAM131C2P, 1 more genes
    nsv3870632copy number variation1nstd102humanBenign GRCh37 chr1: 16,346,507-16,389,026 , GRCh38.p12 chr1: 16,020,012-16,062,531 CLCNKB, FAM131C, 3 more genes
    nsv3872920copy number variation1nstd102humanBenign GRCh37 chr1: 16,336,654-16,377,139 , GRCh38.p12 chr1: 16,010,159-16,050,644 CLCNKB, FAM131C2P, 2 more genes
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