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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140061copy number variation1nstd232human GRCh37.p13 chr9: 113,072,203-113,072,266 , GRCh38.p12 chr9: 110,309,923-110,309,986 TXNDC8
    nsv7097681copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,006,437-113,563,268 , GRCh38.p12 chr9: 110,244,157-110,800,988 LOC107987114, RPS21P5, 7 more genes
    nsv7067795inversion1nstd229human GRCh38 chr9: 110,337,507-110,345,648 , GRCh37.p13 chr9: 113,099,787-113,107,928 TXNDC8
    nsv6869376copy number variation1nstd229human GRCh38 chr9: 110,297,271-110,300,857 , GRCh37.p13 chr9: 113,059,551-113,063,137 TXNDC8
    nsv6868964copy number variation1nstd229human GRCh38 chr9: 110,335,545-110,335,698 , GRCh37.p13 chr9: 113,097,825-113,097,978 TXNDC8
    nsv6864117copy number variation1nstd229human GRCh38 chr9: 110,276,457-110,299,771 , GRCh37.p13 chr9: 113,038,737-113,062,051 LOC107987114, TXNDC8
    nsv6861983copy number variation1nstd229human GRCh38 chr9: 110,335,563-110,359,409 , GRCh37.p13 chr9: 113,097,843-113,121,689 TXNDC8
    nsv6858667copy number variation1nstd229human GRCh38 chr9: 110,337,501-110,395,000 , GRCh37.p13 chr9: 113,099,781-113,157,280 SVEP1, RNU6-1039P, 1 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6572755inversion1nstd223human GRCh38 chr9: 110,302,026-110,303,062 , GRCh37.p13 chr9: 113,064,306-113,065,342 TXNDC8
    nsv6572035inversion1nstd223human GRCh38 chr9: 110,313,202-110,313,363 , GRCh37.p13 chr9: 113,075,482-113,075,643 TXNDC8
    nsv6565356inversion1nstd223human GRCh38 chr9: 110,265,889-110,395,682 , GRCh37.p13 chr9: 113,028,169-113,157,962 SVEP1, TXNDC8, 2 more genes
    nsv6455456copy number variation1nstd223human GRCh38 chr9: 110,291,833-110,302,030 , GRCh37.p13 chr9: 113,054,113-113,064,310 TXNDC8
    nsv6441527copy number variation1nstd223human GRCh38 chr9: 110,190,601-110,309,700 , GRCh37.p13 chr9: 112,952,881-113,071,980 C9orf152, TXN, 3 more genes
    nsv6437552copy number variation1nstd223human GRCh38 chr9: 110,159,107-110,309,502 , GRCh37.p13 chr9: 112,921,387-113,071,782 TXN, TXNDC8, 5 more genes
    nsv6437117copy number variation1nstd223human GRCh38 chr9: 110,321,262-110,322,028 , GRCh37.p13 chr9: 113,083,542-113,084,308 TXNDC8
    nsv6436803copy number variation1nstd223human GRCh38 chr9: 110,251,901-110,316,400 , GRCh37.p13 chr9: 113,014,181-113,078,680 LOC107987114, TXN, 1 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
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