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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098879copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,564,105-2,647,768 , GRCh38.p12 chr16: 2,514,104-2,597,767 CEMP1, AMDHD2, 3 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
    nsv7076133inversion1nstd229human GRCh38 chr16: 2,477,271-2,520,942 , GRCh37.p13 chr16: 2,527,272-2,570,943 AMDHD2, ATP6V0C, 1 more genes
    nsv6974941copy number variation1nstd229human GRCh38 chr16: 2,520,813-2,523,510 , GRCh37.p13 chr16: 2,570,814-2,573,511 AMDHD2
    nsv6971222copy number variation1nstd229human GRCh38 chr16: 2,514,182-2,519,216 , GRCh37.p13 chr16: 2,564,183-2,569,217 ATP6V0C, AMDHD2
    nsv6969026copy number variation1nstd229human GRCh38 chr16: 2,522,782-2,526,384 , GRCh37.p13 chr16: 2,572,783-2,576,385 AMDHD2
    nsv6964063copy number variation1nstd229human GRCh38 chr16: 2,531,103-2,531,140 , GRCh37.p13 chr16: 2,581,104-2,581,141 CEMP1, MIR3178, 1 more genes
    nsv6962230copy number variation1nstd229human GRCh38 chr16: 2,521,125-2,527,558 , GRCh37.p13 chr16: 2,571,126-2,577,559 AMDHD2
    nsv6959102copy number variation1nstd229human GRCh38 chr16: 2,521,808-2,522,710 , GRCh37.p13 chr16: 2,571,809-2,572,711 AMDHD2
    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
    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
    nsv6496277copy number variation1nstd223human GRCh38 chr16: 2,526,138-2,526,154 , GRCh37.p13 chr16: 2,576,139-2,576,155 AMDHD2
    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
    nsv6192005copy number variation1nstd214human GRCh38 chr16: 2,520,576-2,520,637 , GRCh37.p13 chr16: 2,570,577-2,570,638 AMDHD2, ATP6V0C
    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
    nsv6029900copy number variation1nstd212human GRCh38 chr16: 2,522,562-2,522,633 , GRCh37.p13 chr16: 2,572,563-2,572,634 AMDHD2
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