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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146099copy number variation1nstd232human GRCh37.p13 chr16: 4,394,639-4,394,746 , GRCh38.p12 chr16: 4,344,638-4,344,745 PAM16, CORO7-PAM16
    nsv7140979copy number variation1nstd232human GRCh37.p13 chr16: 4,394,657-4,394,746 , GRCh38.p12 chr16: 4,344,656-4,344,745 PAM16, CORO7-PAM16
    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
    nsv6977076copy number variation1nstd229human GRCh38 chr16: 4,212,270-4,606,613 , GRCh37.p13 chr16: 4,262,271-4,656,614 VASN, C16orf96, 13 more genes
    nsv6976423copy number variation1nstd229human GRCh38 chr16: 4,345,125-4,351,214 , GRCh37.p13 chr16: 4,395,126-4,401,215 PAM16, CORO7-PAM16
    nsv6973065copy number variation1nstd229human GRCh38 chr16: 4,343,133-4,347,774 , GRCh37.p13 chr16: 4,393,134-4,397,775 PAM16, CORO7-PAM16
    nsv6969686copy number variation1nstd229human GRCh38 chr16: 4,335,701-4,340,400 , GRCh37.p13 chr16: 4,385,702-4,390,401 CORO7-PAM16, GLIS2, 1 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 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
    nsv6513982copy number variation1nstd223human GRCh38 chr16: 4,342,269-4,342,565 , GRCh37.p13 chr16: 4,392,270-4,392,566 CORO7-PAM16, PAM16
    nsv6509459copy number variation1nstd223human GRCh38 chr16: 4,348,932-4,350,286 , GRCh37.p13 chr16: 4,398,933-4,400,287 CORO7-PAM16, PAM16
    nsv6314863copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,619,617-4,448,281 , GRCh37.p13 chr16: 3,669,618-4,498,282 TRAP1, CORO7-PAM16, 15 more genes
    nsv6309867copy number variation1nstd102humanUncertain significance GRCh37 chr16: 4,390,320-4,391,525 , GRCh38.p12 chr16: 4,340,319-4,341,524 , GRCh38.p12 chr16|NT_187608.1: 40,683-41,888 CORO7-PAM16, PAM16
    nsv6188621copy number variation1nstd214human GRCh38 chr16: 4,344,181-4,344,368 , GRCh37.p13 chr16: 4,394,182-4,394,369 CORO7-PAM16, PAM16
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6132990copy number variation1nstd213human GRCh37 chr16: 3,980,000-5,140,001 , GRCh38.p12 chr16: 3,929,999-5,090,000 ADCY9, HMOX2, 38 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv6099905insertion1nstd212human GRCh38 chr16: 4,344,630-4,344,630 , GRCh37.p13 chr16: 4,394,631-4,394,631 CORO7-PAM16, PAM16
    nsv6098383insertion1nstd212human GRCh38 chr16: 4,344,365-4,344,365 , GRCh37.p13 chr16: 4,394,366-4,394,366 CORO7-PAM16, PAM16
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