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Items: 1 to 20 of 52

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456113copy number variation1nstd102humanPathogenic GRCh37 chr9: 102,965,586-103,023,946 , GRCh38.p12 chr9: 100,203,304-100,261,664 INVS
    nsv6312669copy number variation1nstd102humanPathogenic GRCh37 chr9: 103,027,084-103,035,378 , GRCh38.p12 chr9: 100,264,802-100,273,096 INVS
    nsv6112734copy number variation1nstd102humanPathogenic GRCh37 chr9: 103,059,178-103,060,312 , GRCh38.p12 chr9: 100,296,896-100,298,030 INVS
    nsv6312743copy number variation1nstd102humanPathogenic GRCh37 chr9: 103,014,545-103,015,438 , GRCh38.p12 chr9: 100,252,263-100,253,156 INVS
    nsv3887231copy number variation1nstd102humanPathogenic GRCh37 chr9: 102,888,645-102,888,851 , GRCh38 chr9: 100,126,363-100,126,569 INVS
    nsv5673814copy number variation1nstd102humanPathogenic GRCh37 chr9: 103,008,898-103,009,069 , GRCh38.p12 chr9: 100,246,616-100,246,787 INVS
    nsv3883494copy number variation1nstd102humanPathogenic GRCh37 chr9: 102,866,780-102,866,909 , GRCh38 chr9: 100,104,498-100,104,627 INVS
    nsv6312838copy number variation1nstd102humanUncertain significance GRCh37 chr9: 103,004,832-103,009,089 , GRCh38.p12 chr9: 100,242,550-100,246,807 INVS
    nsv3886152copy number variation1nstd102humanUncertain significance GRCh38 chr9: 100,226,042-100,226,255 , GRCh37 chr9: 102,988,324-102,988,537 INVS
    nsv4728821copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,911,709-103,044,374 , GRCh38.p12 chr9: 100,149,427-100,282,092 INVS, NANOGP5
    nsv3893970copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,909,159-102,988,115 , GRCh38.p12 chr9: 100,146,877-100,225,833 INVS, NANOGP5
    nsv7097916copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,988,324-103,062,956 , GRCh38.p12 chr9: 100,226,042-100,300,674 INVS, TEX10
    nsv3876442copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 102,814,578-102,968,415 , GRCh38.p12 chr9: 100,052,296-100,206,133 INVS, ERP44, 3 more genes
    nsv5381647copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,866,804-103,035,378 , GRCh38.p12 chr9: 100,104,522-100,273,096 INVS, NANOGP5, 1 more genes
    nsv3917989copy number variation1nstd102humanPathogenic GRCh37 chr9: 102,112,198-118,529,754 , NCBI36 chr9: 101,152,019-117,569,575 , GRCh38 chr9: 99,349,916-115,767,475 INVS, CTNNAL1, 262 more genes
    nsv3922633copy number variation2nstd102humanPathogenic GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312 INVS, RAD23B, 262 more genes
    nsv3922551copy number variation1nstd102humanPathogenic GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849 INVS, HEMGN, 243 more genes
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 INVS, SUGT1P4-STRA6LP, 255 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 INVS, RPS26P37, 238 more genes
    nsv3910258copy number variation1nstd102humanPathogenic GRCh38 chr9: 99,024,205-109,947,890 , GRCh37 chr9: 101,786,487-112,710,170 , NCBI36 chr9: 100,826,308-111,749,991 INVS, LOC105376191, 167 more genes
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