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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098906copy number variation1nstd102humanUncertain significance GRCh38 chr16: 3,499,966-3,774,794 , GRCh37.p13 chr16: 3,549,966-3,824,795 CLUAP1, LOC105371060, 6 more genes
    nsv7095018copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,565,488-3,801,827 , GRCh38.p12 chr16: 3,515,488-3,751,826 TRAP1, NLRC3, 6 more genes
    nsv7094839copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,586,102-3,658,965 , GRCh38.p12 chr16: 3,536,102-3,608,964 NLRC3, LOC105371060, 3 more genes
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094582copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,551,068-3,901,030 , GRCh38.p12 chr16: 3,501,068-3,851,029 NLRC3, LOC105371060, 6 more genes
    nsv7059322inversion1nstd229human GRCh38 chr16: 3,560,683-3,614,402 , GRCh37.p13 chr16: 3,610,684-3,664,403 DNASE1, NLRC3, 2 more genes
    nsv6974168copy number variation1nstd229human GRCh38 chr16: 3,542,201-3,575,000 , GRCh37.p13 chr16: 3,592,201-3,625,001 NLRC3, LOC101929732
    nsv6970028copy number variation1nstd229human GRCh38 chr16: 3,565,831-3,573,208 , GRCh37.p13 chr16: 3,615,832-3,623,209 NLRC3
    nsv6968673copy number variation1nstd229human GRCh38 chr16: 3,514,969-3,753,257 , GRCh37.p13 chr16: 3,564,969-3,803,258 CREBBP, SLX4, 6 more genes
    nsv6965660copy number variation1nstd229human GRCh38 chr16: 3,558,001-3,561,200 , GRCh37.p13 chr16: 3,608,002-3,611,201 LOC101929732, NLRC3
    nsv6964540copy number variation1nstd229human GRCh38 chr16: 3,576,998-3,595,076 , GRCh37.p13 chr16: 3,626,999-3,645,077 NLRC3, LOC105371060, 1 more genes
    nsv6963623copy number variation1nstd229human GRCh38 chr16: 3,573,475-3,580,801 , GRCh37.p13 chr16: 3,623,476-3,630,802 SLX4, NLRC3, 1 more genes
    nsv6963189copy number variation1nstd229human GRCh38 chr16: 3,575,501-3,600,000 , GRCh37.p13 chr16: 3,625,502-3,650,001 NLRC3, LOC105371060, 1 more genes
    nsv6959539copy number variation1nstd229human GRCh38 chr16: 3,567,537-3,581,568 , GRCh37.p13 chr16: 3,617,538-3,631,569 LOC105371060, SLX4, 1 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6623670copy number variation1nstd224human GRCh37 chr16: 3,575,270-3,598,190 , GRCh38.p12 chr16: 3,525,270-3,548,190 NLRC3, LOC101929732, 1 more genes
    nsv6623626copy number variation1nstd224human GRCh37 chr16: 3,598,190-3,614,971 , GRCh38.p12 chr16: 3,548,190-3,564,970 NLRC3, LOC101929732
    nsv6623222copy number variation1nstd224human GRCh37 chr16: 3,594,296-3,614,971 , GRCh38.p12 chr16: 3,544,296-3,564,970 NLRC3, LOC101929732
    nsv6586639inversion1nstd223human GRCh38 chr16: 3,555,416-3,555,718 , GRCh37.p13 chr16: 3,605,417-3,605,719 LOC101929732, NLRC3
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