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Items: 1 to 20 of 227

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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
    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
    nsv6505384copy number variation1nstd223human GRCh38 chr16: 2,463,611-2,466,619 , GRCh37.p13 chr16: 2,513,612-2,516,620 TEDC2-AS1, MIR6768, 1 more genes
    nsv6498790copy number variation1nstd223human GRCh38 chr16: 2,334,094-2,648,283 , GRCh37.p13 chr16: 2,384,095-2,698,284 LOC105371050, NTN3, 16 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
    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
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133016copy number variation1nstd213human GRCh37 chr16: 2,450,000-2,590,001 , GRCh38.p12 chr16: 2,399,999-2,540,000 ATP6V0C, CCNF, 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
    nsv6022653copy number variation1nstd212human GRCh38 chr16: 2,458,160-2,462,474 , GRCh37.p13 chr16: 2,508,161-2,512,475 CCNF, TEDC2, 2 more genes
    nsv5931994copy number variation1nstd209human GRCh38 chr16: 2,458,156-2,462,474 , GRCh37.p13 chr16: 2,508,157-2,512,475 MIR6768, TEDC2, 2 more genes
    nsv5868708copy number variation1nstd209human GRCh38 chr16: 2,457,970-2,462,419 , GRCh37.p13 chr16: 2,507,971-2,512,420 LOC105371050, CCNF, 2 more genes
    nsv5532228copy number variation1nstd206human GRCh38 chr16: 2,458,116-2,462,519 , GRCh37.p13 chr16: 2,508,117-2,512,520 CCNF, LOC105371050, 2 more genes
    nsv5380995copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978 TEDC2, MIR3677HG, 33 more genes
    nsv5271510copy number variation1nstd204human GRCh38.p13 chr16: 2,443,001-2,620,300 , GRCh37.p13 chr16: 2,493,002-2,670,301 LOC652276, PDPK1, 13 more genes
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5266471copy number variation1nstd204human GRCh38.p13 chr16: 1,936,501-2,552,200 , GRCh37.p13 chr16: 1,986,502-2,602,201 AMDHD2, MIR3178, 56 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5009356copy number variation1nstd200human GRCh38 chr16: 2,441,806-2,459,934 , GRCh37.p13 chr16: 2,491,807-2,509,935 TEDC2, MIR6767, 2 more genes
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