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Items: 1 to 20 of 715

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145960copy number variation1nstd232human GRCh37.p13 chr9: 133,040,090-133,040,221 , GRCh38.p12 chr9: 130,277,811-130,277,942 HMCN2
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7074692inversion1nstd229human GRCh38 chr9: 130,371,805-130,371,854 , GRCh37.p13 chr9: 133,247,192-133,247,241 HMCN2
    nsv7072154inversion1nstd229human GRCh38 chr9: 130,289,499-130,301,117 , GRCh37.p13 chr9: 133,051,778-133,063,396 , GRCh37.p13 chr9|NW_004070869.1: 158,929-170,547 HMCN2
    nsv7068458inversion1nstd229human GRCh38 chr9: 130,280,899-130,310,097 , GRCh37.p13 chr9: 133,043,178-133,072,376 , GRCh37.p13 chr9|NW_004070869.1: 150,329-179,527 HMCN2
    nsv6877782copy number variation1nstd229human GRCh38 chr9: 130,349,176-130,349,342 , GRCh37.p13 chr9: 133,224,563-133,224,729 HMCN2
    nsv6877565copy number variation1nstd229human GRCh38 chr9: 130,162,901-130,666,900 , GRCh37.p13 chr9: 133,223,061-133,542,287 MIR6856, LOC107987134, 9 more genes
    nsv6877393copy number variation1nstd229human GRCh38 chr9: 130,388,728-130,388,746 , GRCh37.p13 chr9: 133,264,115-133,264,133 HMCN2
    nsv6876658copy number variation1nstd229human GRCh38 chr9: 130,276,388-130,277,223 , GRCh37.p13 chr9: 133,038,667-133,039,502 , GRCh37.p13 chr9|NW_004070869.1: 145,818-146,653 HMCN2
    nsv6875602copy number variation1nstd229human GRCh38 chr9: 130,414,695-130,417,856 , GRCh37.p13 chr9: 133,290,082-133,293,243 HMCN2
    nsv6873727copy number variation1nstd229human GRCh38 chr9: 130,301,201-130,310,100 , GRCh37.p13 chr9|NW_004070869.1: 170,631-179,530 , GRCh37.p13 chr9: 133,063,480-133,072,379 HMCN2
    nsv6873564copy number variation1nstd229human GRCh38 chr9: 130,419,670-130,419,743 , GRCh37.p13 chr9: 133,295,057-133,295,130 LOC107987134, HMCN2
    nsv6872885copy number variation1nstd229human GRCh38 chr9: 130,290,495-130,293,131 , GRCh37.p13 chr9: 133,052,774-133,055,410 , GRCh37.p13 chr9|NW_004070869.1: 159,925-162,561 HMCN2
    nsv6872702copy number variation1nstd229human GRCh38 chr9: 130,313,094-130,313,425 , GRCh37.p13 chr9|NW_004070869.1: 182,524-182,855 HMCN2
    nsv6872688copy number variation1nstd229human GRCh38 chr9: 130,314,217-130,315,030 , GRCh37.p13 chr9|NW_004070869.1: 183,647-184,460 HMCN2
    nsv6872488copy number variation1nstd229human GRCh38 chr9: 130,421,097-130,581,801 , GRCh37.p13 chr9: 133,296,484-133,457,188 LOC100272217, ASS1, 3 more genes
    nsv6871927copy number variation1nstd229human GRCh38 chr9: 130,410,528-130,428,606 , GRCh37.p13 chr9: 133,285,915-133,303,993 HMCN2, LOC107987134
    nsv6871626copy number variation1nstd229human GRCh38 chr9: 130,327,607-130,330,391 , GRCh37.p13 chr9|NW_004070869.1: 197,037-199,821 HMCN2
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