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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv6731687copy number variation1nstd229human GRCh38 chr3: 169,773,099-169,962,497 , GRCh37.p13 chr3: 169,490,887-169,680,285 MYNN, LRRC34, 6 more genes
    nsv6728752copy number variation1nstd229human GRCh38 chr3: 169,748,422-169,802,383 , GRCh37.p13 chr3: 169,466,210-169,520,171 TERC, TRV-AAC1-1, 3 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636764copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,718,767-169,662,001 , GRCh38.p12 chr3: 169,000,979-169,944,213 LRRIQ4, MECOM, 17 more genes
    nsv6373985copy number variation1nstd223human GRCh38 chr3: 169,763,201-169,777,100 , GRCh37.p13 chr3: 169,480,989-169,494,888 ACTRT3, MYNN, 2 more genes
    nsv6372501copy number variation1nstd223human GRCh38 chr3: 169,774,088-169,776,925 , GRCh37.p13 chr3: 169,491,876-169,494,713 MYNN
    nsv6367562copy number variation1nstd223human GRCh38 chr3: 169,762,301-169,777,000 , GRCh37.p13 chr3: 169,480,089-169,494,788 MYNN, ACTRT3, 2 more genes
    nsv6311968copy number variation1nstd102humanUncertain significance GRCh37 chr3: 169,482,388-170,130,102 , GRCh38.p12 chr3: 169,764,600-170,412,314 TRV-AAC1-1, SEC62, 19 more genes
    nsv6291110copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 168,118,411-179,867,071 , GRCh38.p12 chr3: 168,400,623-180,149,283 ACTL6A, ECT2, 141 more genes
    nsv6282610insertion2nstd214human GRCh38 chr3: 169,771,493-169,771,493 , GRCh37.p13 chr3: 169,489,281-169,489,281 MYNN, TRV-AAC1-1
    nsv6161157copy number variation1nstd214human GRCh38 chr3: 169,771,462-169,771,523 , GRCh37.p13 chr3: 169,489,250-169,489,311 MYNN, TRV-AAC1-1
    nsv6158904copy number variation1nstd214human GRCh38 chr3: 169,771,406-169,771,492 , GRCh37.p13 chr3: 169,489,194-169,489,280 MYNN, TRV-AAC1-1
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv6078810insertion1nstd212human GRCh38 chr3: 169,782,022-169,782,022 , GRCh37.p13 chr3: 169,499,810-169,499,810 MYNN
    nsv6068947insertion1nstd212human GRCh38 chr3: 169,771,483-169,771,483 , GRCh37.p13 chr3: 169,489,271-169,489,271 MYNN, TRV-AAC1-1
    nsv5684694mobile element insertion2nstd211human GRCh38 chr3: 169,784,017-169,784,017 , GRCh37.p13 chr3: 169,501,805-169,501,805 MYNN
    nsv5605847insertion1nstd207human GRCh38 chr3: 169,771,429-169,771,429 , GRCh37.p13 chr3: 169,489,217-169,489,217 TRV-AAC1-1, MYNN
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
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