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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099223copy number variation1nstd231human GRCh38.p12 chr1: 108,551,579-110,710,631 , GRCh37 chr1: 109,094,201-111,253,253 ALX3, AMPD2, 74 more genes
    nsv7095739copy number variation1nstd102humanPathogenic GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554 RPL7L1P21, GSTM4, 90 more genes
    nsv7095695copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,145,905-114,454,813 , GRCh38.p12 chr1: 110,603,283-113,912,191 LOC107985189, RNU6-792P, 83 more genes
    nsv7057025inversion1nstd229human GRCh38 chr1: 110,649,253-110,686,965 , GRCh37.p13 chr1: 111,191,875-111,229,587 KCNA3, LOC107985174
    nsv6639591copy number variation1nstd229human GRCh38 chr1: 110,648,706-110,652,393 , GRCh37.p13 chr1: 111,191,328-111,195,015 KCNA3, LOC107985174
    nsv6636999copy number variation1nstd102humanUncertain significance GRCh37 chr1: 110,662,135-111,401,322 , GRCh38.p12 chr1: 110,119,513-110,858,700 LOC105378898, CYMP, 19 more genes
    nsv6535928inversion1nstd223human GRCh38 chr1: 110,649,210-110,686,968 , GRCh37.p13 chr1: 111,191,832-111,229,590 LOC107985174, KCNA3
    nsv6334907copy number variation1nstd223human GRCh38 chr1: 110,654,801-110,656,200 , GRCh37.p13 chr1: 111,197,423-111,198,822 KCNA3, LOC107985174
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6133729copy number variation1nstd213human GRCh37 chr1: 110,680,000-111,480,001 , GRCh38.p12 chr1: 110,137,378-110,937,379 KCNA2, SLC16A4, 21 more genes
    nsv5980520copy number variation1nstd212human GRCh38 chr1: 110,652,567-110,652,731 , GRCh37.p13 chr1: 111,195,189-111,195,353 LOC107985174, KCNA3
    nsv5883325copy number variation1nstd209human GRCh38 chr1: 110,659,868-110,660,150 , GRCh37.p13 chr1: 111,202,490-111,202,772 KCNA3, LOC107985174
    nsv5693588mobile element insertion2nstd211human GRCh38 chr1: 110,672,866-110,672,866 , GRCh37.p13 chr1: 111,215,488-111,215,488 LOC107985174, KCNA3
    nsv5395290mobile element insertion1nstd206human GRCh38 chr1: 110,672,866-110,672,917 , GRCh37.p13 chr1: 111,215,488-111,215,539 LOC107985174, KCNA3
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5031598inversion1nstd200human GRCh38 chr1: 110,649,252-110,686,967 , GRCh37.p13 chr1: 111,191,874-111,229,589 LOC107985174, KCNA3
    nsv4894409copy number variation1nstd200human GRCh38 chr1: 110,569,134-110,720,529 , GRCh37.p13 chr1: 111,111,756-111,263,151 KCNA2, KCNA3, 1 more genes
    nsv4890749copy number variation1nstd200human GRCh38 chr1: 110,648,706-110,652,385 , GRCh37.p13 chr1: 111,191,328-111,195,007 KCNA3, LOC107985174
    nsv4869663inversion1nstd200human GRCh37 chr1: 111,191,874-111,229,589 , GRCh38.p12 chr1: 110,649,252-110,686,967 KCNA3, LOC107985174
    nsv4781116copy number variation1nstd200human GRCh37 chr1: 111,111,756-111,263,151 , GRCh38.p12 chr1: 110,569,134-110,720,529 KCNA3, LOC107985174, 1 more genes
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