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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7098189copy number variation1nstd102humanUncertain significance GRCh37 chr8: 97,156,791-97,345,794 , GRCh38.p12 chr8: 96,144,563-96,333,566 UQCRB-AS1, MTERF3, 4 more genes
    nsv7097674copy number variation1nstd102humanUncertain significance GRCh37 chr8: 96,037,237-97,345,794 , GRCh38.p12 chr8: 95,025,009-96,333,566 NDUFAF6, LINC01298, 19 more genes
    nsv7072181inversion1nstd229human GRCh38 chr8: 94,465,642-98,351,757 , GRCh37.p13 chr8: 95,477,870-99,363,985 SDC2, LOC100286997, 59 more genes
    nsv7070574inversion1nstd229human GRCh38 chr8: 96,129,608-96,149,737 , GRCh37.p13 chr8: 97,141,836-97,161,965 GDF6
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6421066copy number variation1nstd223human GRCh38 chr8: 96,145,701-96,147,100 , GRCh37.p13 chr8: 97,157,929-97,159,328 GDF6
    nsv6420283copy number variation1nstd223human GRCh38 chr8: 96,136,158-96,225,602 , GRCh37.p13 chr8: 97,148,386-97,237,830 UQCRB, GDF6
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6137320copy number variation1nstd213human GRCh37 chr8: 96,440,000-102,500,001 , GRCh38.p12 chr8: 95,427,772-101,487,773 SDC2, RGS22, 102 more genes
    nsv6136709copy number variation1nstd213human GRCh37 chr8: 94,750,000-101,120,001 , GRCh38.p12 chr8: 93,737,772-100,107,773 SDC2, STK3, 101 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6015429copy number variation1nstd212human GRCh38 chr8: 96,156,363-96,156,416 , GRCh37.p13 chr8: 97,168,591-97,168,644 GDF6
    nsv6008508copy number variation1nstd212human GRCh38 chr8: 96,147,254-96,147,492 , GRCh37.p13 chr8: 97,159,482-97,159,720 GDF6
    nsv5912852copy number variation1nstd209human GRCh38 chr8: 96,145,964-96,147,140 , GRCh37.p13 chr8: 97,158,192-97,159,368 GDF6
    nsv5372026translocation1nstd200human GRCh38 chr8: 96,148,533-96,148,533 , GRCh38 chr8: 96,150,479-96,150,479 , GRCh37.p13 chr8: 97,160,761-97,160,761 , GRCh37.p13 chr8: 97,162,707-97,162,707 GDF6
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