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Items: 1 to 20 of 394

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv6970635copy number variation1nstd229human GRCh38 chr16: 2,188,965-2,194,627 , GRCh37.p13 chr16: 2,238,966-2,244,628 CASKIN1
    nsv6970383copy number variation1nstd229human GRCh38 chr16: 2,180,703-2,238,122 , GRCh37.p13 chr16: 2,230,704-2,288,123 E4F1, CASKIN1, 5 more genes
    nsv6968410copy number variation1nstd229human GRCh38 chr16: 2,175,846-2,191,742 , GRCh37.p13 chr16: 2,225,847-2,241,743 CASKIN1, TRAF7
    nsv6959164copy number variation1nstd229human GRCh38 chr16: 1,882,476-2,224,508 , GRCh37.p13 chr16: 1,932,477-2,274,509 SNORD60, NTHL1, 35 more genes
    nsv6958935copy number variation1nstd229human GRCh38 chr16: 1,975,501-2,237,700 , GRCh37.p13 chr16: 2,025,502-2,287,701 BRICD5, MLST8, 25 more genes
    nsv6638000copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 2,106,895-2,227,470 , GRCh38.p12 chr16: 2,056,894-2,177,469 PKD1, TSC2, 10 more genes
    nsv6637664copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,266,791 , GRCh38.p12 chr16: 1,971,143-2,216,790 SNHG19, MIR6511B1, 22 more genes
    nsv6637330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,942,430-2,653,144 , GRCh38.p12 chr16: 1,892,429-2,603,143 SNHG19, SNHG9, 58 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
    nsv6315012copy number variation1nstd102humanPathogenic GRCh38 chr16: 2,066,081-2,241,220 , GRCh37.p13 chr16: 2,116,082-2,291,221 CASKIN1, PKD1, 16 more genes
    nsv6315010copy number variation1nstd102humanPathogenic GRCh38 chr16: 2,047,157-2,220,112 , GRCh37.p13 chr16: 2,097,158-2,270,113 RAB26, BRICD5, 14 more genes
    nsv6314182copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,847,662-2,653,144 , GRCh38.p12 chr16: 1,797,661-2,603,143 CASKIN1, RPL3L, 63 more genes
    nsv6307328copy number variation1nstd186human GRCh37 chr16: 2,206,001-2,262,001 , GRCh38.p12 chr16: 2,156,000-2,212,000 CASKIN1, MLST8, 3 more genes
    nsv6291471copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,830,141-2,592,737 , GRCh38.p12 chr16: 1,780,140-2,542,736 CEMP1, NTN3, 65 more genes
    nsv6274646copy number variation1nstd214human GRCh38 chr16: 2,178,786-2,178,845 , GRCh37.p13 chr16: 2,228,787-2,228,846 CASKIN1
    nsv6270774copy number variation1nstd214human GRCh38 chr16: 2,189,779-2,189,830 , GRCh37.p13 chr16: 2,239,780-2,239,831 CASKIN1
    nsv6144571copy number variation1nstd206human GRCh38 chr16: 2,156,000-2,212,000 , GRCh37.p13 chr16: 2,206,001-2,262,001 BRICD5, MLST8, 3 more genes
    nsv6133285copy number variation1nstd213human GRCh37 chr16: 850,000-2,500,001 , GRCh38.p12 chr16: 800,000-2,450,000 ABCA3, CCNF, 101 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
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