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Items: 1 to 20 of 371

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129750insertion1nstd186human GRCh37 chr14: 77,701,810-77,701,860 , GRCh38.p12 chr14: 77,235,467-77,235,517 TMEM63C
    nsv6120802copy number variation1nstd186human GRCh37 chr14: 77,686,872-77,687,555 , GRCh38.p12 chr14: 77,220,529-77,221,212 TMEM63C
    nsv5973753insertion1nstd209human GRCh38 chr14: 77,186,801-77,186,801 , GRCh37.p13 chr14: 77,653,144-77,653,144 TMEM63C
    nsv5969558insertion1nstd209human GRCh38 chr14: 77,215,614-77,215,614 , GRCh37.p13 chr14: 77,681,957-77,681,957 TMEM63C
    nsv5947015copy number variation1nstd209human GRCh38 chr14: 77,208,286-77,208,573 , GRCh37.p13 chr14: 77,674,629-77,674,916 TMEM63C
    nsv5941412copy number variation1nstd209human GRCh38 chr14: 77,193,244-77,193,343 , GRCh37.p13 chr14: 77,659,587-77,659,686 TMEM63C
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5929040copy number variation1nstd209human GRCh38 chr14: 77,220,922-77,221,294 , GRCh37.p13 chr14: 77,687,265-77,687,637 TMEM63C
    nsv5663293insertion1nstd207human GRCh38 chr14: 77,235,624-77,235,624 , GRCh37.p13 chr14: 77,701,967-77,701,967 TMEM63C
    nsv5660837insertion1nstd207human GRCh38 chr14: 77,236,261-77,236,261 , GRCh37.p13 chr14: 77,702,604-77,702,604 TMEM63C
    nsv5660238insertion1nstd207human GRCh38 chr14: 77,236,016-77,236,016 , GRCh37.p13 chr14: 77,702,359-77,702,359 TMEM63C
    nsv5659224insertion2nstd207human GRCh38 chr14: 77,220,916-77,220,916 , GRCh37.p13 chr14: 77,687,259-77,687,259 TMEM63C
    nsv5658879insertion1nstd207human GRCh38 chr14: 77,235,534-77,235,534 , GRCh37.p13 chr14: 77,701,877-77,701,877 TMEM63C
    nsv5656839insertion1nstd207human GRCh38 chr14: 77,236,123-77,236,123 , GRCh37.p13 chr14: 77,702,466-77,702,466 TMEM63C
    nsv5656450insertion1nstd207human GRCh38 chr14: 77,236,382-77,236,382 , GRCh37.p13 chr14: 77,702,725-77,702,725 TMEM63C
    nsv5648510insertion1nstd207human GRCh38 chr14: 77,221,341-77,221,341 , GRCh37.p13 chr14: 77,687,684-77,687,684 TMEM63C
    nsv5599063copy number variation1nstd207human GRCh38 chr14: 77,235,509-77,235,710 , GRCh37.p13 chr14: 77,701,852-77,702,053 TMEM63C
    nsv5597417copy number variation1nstd207human GRCh38 chr14: 77,235,894-77,235,989 , GRCh37.p13 chr14: 77,702,237-77,702,332 TMEM63C
    nsv5585884copy number variation1nstd207human GRCh38 chr14: 77,220,922-77,221,294 , GRCh37.p13 chr14: 77,687,265-77,687,637 TMEM63C
    nsv5585809copy number variation1nstd207human GRCh38 chr14: 77,221,077-77,221,150 , GRCh37.p13 chr14: 77,687,420-77,687,493 TMEM63C
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