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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7073824inversion1nstd229human GRCh38 chr8: 101,973,771-102,089,174 , GRCh37.p13 chr8: 102,985,999-103,101,402 LOC104054148, NCALD
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7064861inversion1nstd229human GRCh38 chr8: 101,974,141-102,026,392 , GRCh37.p13 chr8: 102,986,369-103,038,620 NCALD, LOC104054148
    nsv6857955copy number variation1nstd229human GRCh38 chr8: 101,982,043-101,988,662 , GRCh37.p13 chr8: 102,994,271-103,000,890 LOC104054148, NCALD
    nsv6857338copy number variation1nstd229human GRCh38 chr8: 101,978,196-101,995,069 , GRCh37.p13 chr8: 102,990,424-103,007,297 LOC104054148, NCALD
    nsv6851447copy number variation1nstd229human GRCh38 chr8: 101,993,334-101,999,002 , GRCh37.p13 chr8: 103,005,562-103,011,230 NCALD, LOC104054148
    nsv6845132copy number variation1nstd229human GRCh38 chr8: 101,987,437-101,990,972 , GRCh37.p13 chr8: 102,999,665-103,003,200 LOC104054148, NCALD
    nsv6844340copy number variation1nstd229human GRCh38 chr8: 101,981,260-101,985,153 , GRCh37.p13 chr8: 102,993,488-102,997,381 NCALD, LOC104054148
    nsv6841335copy number variation1nstd229human GRCh38 chr8: 101,991,219-101,991,424 , GRCh37.p13 chr8: 103,003,447-103,003,652 LOC104054148, NCALD
    nsv6841127copy number variation1nstd229human GRCh38 chr8: 101,986,657-101,998,476 , GRCh37.p13 chr8: 102,998,885-103,010,704 NCALD, LOC104054148
    nsv6839804copy number variation1nstd229human GRCh38 chr8: 101,983,143-101,983,510 , GRCh37.p13 chr8: 102,995,371-102,995,738 NCALD, LOC104054148
    nsv6838600copy number variation1nstd229human GRCh38 chr8: 101,943,801-102,127,000 , GRCh37.p13 chr8: 102,956,029-103,139,228 MIR5680, LOC104054148, 1 more genes
    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
    nsv6425785copy number variation1nstd223human GRCh38 chr8: 101,986,656-101,998,475 , GRCh37.p13 chr8: 102,998,884-103,010,703 NCALD, LOC104054148
    nsv6420634copy number variation1nstd223human GRCh38 chr8: 101,987,507-101,988,744 , GRCh37.p13 chr8: 102,999,735-103,000,972 LOC104054148, NCALD
    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
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