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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146937copy number variation1nstd232human GRCh37.p13 chr1: 197,682,902-197,682,965 , GRCh38.p12 chr1: 197,713,772-197,713,835 DENND1B
    nsv7145330insertion1nstd232human GRCh37.p13 chr1: 197,514,066-197,514,066 , GRCh38.p12 chr1: 197,544,936-197,544,936 DENND1B
    nsv7142716copy number variation1nstd232human GRCh37.p13 chr1: 197,501,316-197,501,385 , GRCh38.p12 chr1: 197,532,186-197,532,255 DENND1B
    nsv7138970insertion1nstd232human GRCh37.p13 chr1: 197,500,520-197,500,520 , GRCh38.p12 chr1: 197,531,390-197,531,390 DENND1B
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7093373copy number variation1nstd102humanUncertain significance GRCh37 chr1: 196,670,448-197,898,389 , GRCh38.p12 chr1: 196,701,318-197,929,259 LHX9, ASPM, 19 more genes
    nsv7056334inversion1nstd229human GRCh38 chr1: 197,739,513-197,739,540 , GRCh37.p13 chr1: 197,708,643-197,708,670 DENND1B
    nsv7046755inversion1nstd229human GRCh38 chr1: 197,153,978-198,848,199 , GRCh37.p13 chr1: 197,123,108-198,817,328 FAM204BP, RPL24P5, 15 more genes
    nsv7044345inversion1nstd229human GRCh38 chr1: 196,256,799-197,729,314 , GRCh37.p13 chr1: 196,225,929-197,698,444 EEF1A1P32, MIR4735, 17 more genes
    nsv7038363inversion1nstd229human GRCh38 chr1: 197,669,120-197,669,136 , GRCh37.p13 chr1: 197,638,250-197,638,266 DENND1B
    nsv6677434copy number variation1nstd229human GRCh38 chr1: 197,681,101-197,691,500 , GRCh37.p13 chr1: 197,650,231-197,660,630 EEF1A1P32, DENND1B
    nsv6676500copy number variation1nstd229human GRCh38 chr1: 197,757,004-197,765,416 , GRCh37.p13 chr1: 197,726,134-197,734,546 DENND1B
    nsv6675808copy number variation1nstd229human GRCh38 chr1: 197,677,127-197,677,823 , GRCh37.p13 chr1: 197,646,257-197,646,953 DENND1B
    nsv6674697copy number variation1nstd229human GRCh38 chr1: 197,752,540-197,758,345 , GRCh37.p13 chr1: 197,721,670-197,727,475 DENND1B
    nsv6673972copy number variation1nstd229human GRCh38 chr1: 197,727,242-197,774,620 , GRCh37.p13 chr1: 197,696,372-197,743,750 DENND1B, FAM204BP, 1 more genes
    nsv6673315copy number variation1nstd229human GRCh38 chr1: 197,642,537-197,670,558 , GRCh37.p13 chr1: 197,611,667-197,639,688 DENND1B
    nsv6673255copy number variation1nstd229human GRCh38 chr1: 197,553,677-197,553,742 , GRCh37.p13 chr1: 197,522,807-197,522,872 DENND1B
    nsv6673066copy number variation1nstd229human GRCh38 chr1: 197,516,435-197,528,215 , GRCh37.p13 chr1: 197,485,565-197,497,345 DENND1B
    nsv6670809copy number variation1nstd229human GRCh38 chr1: 197,717,452-197,730,549 , GRCh37.p13 chr1: 197,686,582-197,699,679 DENND1B
    nsv6669574copy number variation1nstd229human GRCh38 chr1: 197,566,701-197,569,700 , GRCh37.p13 chr1: 197,535,831-197,538,830 DENND1B
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