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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7066174inversion1nstd229human GRCh38 chr16: 3,329,626-3,391,593 , GRCh37.p13 chr16: 3,379,626-3,441,593 MTRNR2L4, ZSCAN32, 6 more genes
    nsv6973639copy number variation1nstd229human GRCh38 chr16: 3,389,801-3,396,100 , GRCh37.p13 chr16: 3,439,801-3,446,100 ZSCAN32, LOC105371059
    nsv6970484copy number variation1nstd229human GRCh38 chr16: 3,351,095-3,427,692 , GRCh37.p13 chr16: 3,401,095-3,477,692 MTND2P34, MTRNR2L4, 7 more genes
    nsv6968778copy number variation1nstd229human GRCh38 chr16: 3,206,227-3,444,939 , GRCh37.p13 chr16: 3,256,227-3,494,939 MEFV, ZNF597, 18 more genes
    nsv6966776copy number variation1nstd229human GRCh38 chr16: 3,400,341-3,408,489 , GRCh37.p13 chr16: 3,450,341-3,458,489 ZNF174, ZSCAN32
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6513898copy number variation1nstd223human GRCh38 chr16: 3,357,783-3,391,480 , GRCh37.p13 chr16: 3,407,783-3,441,480 OR2C1, ZSCAN32, 6 more genes
    nsv6509003copy number variation1nstd223human GRCh38 chr16: 3,351,095-3,427,692 , GRCh37.p13 chr16: 3,401,095-3,477,692 LOC105371059, OR2C1, 7 more genes
    nsv6310074copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,293,141-3,929,917 , GRCh38.p12 chr16: 3,243,141-3,879,916 MTRNR2L4, TRAP1, 26 more genes
    nsv6290044copy number variation1nstd218human GRCh38.p12 chr16: 2,757,479-3,781,321 , GRCh37 chr16: 2,807,480-3,831,322 , CREBBP, 87 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133274copy number variation1nstd213human GRCh37 chr16: 2,660,000-3,710,001 , GRCh38.p12 chr16: 2,609,999-3,660,000 DNASE1, MEFV, 90 more genes
    nsv6133023copy number variation1nstd213human GRCh37 chr16: 3,410,000-3,550,001 , GRCh38.p12 chr16: 3,360,000-3,500,001 ZNF174, CLUAP1, 12 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
    nsv6095939insertion1nstd212human GRCh38 chr16: 3,393,207-3,393,207 , GRCh37.p13 chr16: 3,443,207-3,443,207 LOC105371059, ZSCAN32
    nsv5971532insertion1nstd209human GRCh38 chr16: 3,393,227-3,393,227 , GRCh37.p13 chr16: 3,443,227-3,443,227 LOC105371059, ZSCAN32
    nsv5654733insertion2nstd207human GRCh38 chr16: 3,393,202-3,393,202 , GRCh37.p13 chr16: 3,443,202-3,443,202 ZSCAN32, LOC105371059
    nsv5649810insertion1nstd207human GRCh38 chr16: 3,393,239-3,393,239 , GRCh37.p13 chr16: 3,443,239-3,443,239 LOC105371059, ZSCAN32
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