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Items: 1 to 20 of 37

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891722copy number variation1nstd102humanPathogenic GRCh37 chr9: 104,604,851-126,253,089 , GRCh38.p12 chr9: 101,842,569-123,490,810 KLF4, LOC107987013, 326 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 KLF4, 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 KLF4, 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 KLF4, HEMGN, 243 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 KLF4, LOC105376191, 167 more genes
    nsv3891403copy number variation1nstd102humanPathogenic GRCh37 chr9: 103,271,401-113,948,226 , GRCh38.p12 chr9: 100,509,119-111,185,946 KLF4, LOC112268038, 158 more genes
    nsv3916125copy number variation1nstd102humanPathogenic GRCh38 chr9: 103,767,420-112,984,794 , NCBI36 chr9: 105,569,522-114,786,895 , GRCh37 chr9: 106,529,701-115,747,074 KLF4, FRRS1L, 149 more genes
    nsv3895960copy number variation1nstd102humanPathogenic GRCh37 chr9: 106,487,247-114,541,579 , GRCh38.p12 chr9: 103,724,965-111,779,299 KLF4, LOC105376196, 128 more genes
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 KLF4, ACTL7B, 88 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 KLF4, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 KLF4, TBC1D13, 2183 more genes
    nsv3905118copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645 KLF4, MIR219A2, 2183 more genes
    nsv3891842copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222 KLF4, OR13C1P, 2183 more genes
    nsv3895453copy number variation1nstd102humanPathogenic GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039 KLF4, RPL19P15, 2176 more genes
    nsv3900967copy number variation1nstd102humanPathogenic GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664 KLF4, BANCR, 2173 more genes
    nsv3907479copy number variation1nstd102humanPathogenic GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955 KLF4, OR2AM1P, 2174 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 KLF4, TDRD7, 2170 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 KLF4, LOC107987031, 2169 more genes
    nsv3915973copy number variation2nstd102humanPathogenic GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346 KLF4, CTNNAL1, 2170 more genes
    nsv3911025copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976 KLF4, RORB-AS1, 2168 more genes
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