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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7097416copy number variation1nstd102humanPathogenic GRCh37 chr8: 117,859,739-120,844,804 , GRCh38.p12 chr8: 116,847,500-119,832,564 SAMD12, LOC105375717, 38 more genes
    nsv7097415copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,647,788-120,797,526 , GRCh38.p12 chr8: 116,635,549-119,785,286 LOC100286746, LOC105375717, 40 more genes
    nsv7072142inversion1nstd229human GRCh38 chr8: 113,332,988-120,659,210 , GRCh37.p13 chr8: 114,345,217-121,671,450 ENPP2, RAD21-AS1, 67 more genes
    nsv7069706inversion1nstd229human GRCh38 chr8: 117,107,451-117,117,270 , GRCh37.p13 chr8: 118,119,690-118,129,509 SLC30A8, LOC105375716, 1 more genes
    nsv6857749copy number variation1nstd229human GRCh38 chr8: 117,129,101-117,134,100 , GRCh37.p13 chr8: 118,141,340-118,146,339 LOC105375716, SLC30A8
    nsv6857311copy number variation1nstd229human GRCh38 chr8: 116,989,508-116,991,812 , GRCh37.p13 chr8: 118,001,747-118,004,051 SLC30A8
    nsv6857187copy number variation1nstd229human GRCh38 chr8: 117,165,288-117,165,571 , GRCh37.p13 chr8: 118,177,527-118,177,810 SLC30A8, LOC105375716
    nsv6857097copy number variation1nstd229human GRCh38 chr8: 117,077,666-117,081,373 , GRCh37.p13 chr8: 118,089,905-118,093,612 SLC30A8
    nsv6855832copy number variation1nstd229human GRCh38 chr8: 117,110,101-117,114,300 , GRCh37.p13 chr8: 118,122,340-118,126,539 SLC30A8, LOC105375716, 1 more genes
    nsv6854355copy number variation1nstd229human GRCh38 chr8: 116,961,397-116,963,084 , GRCh37.p13 chr8: 117,973,636-117,975,323 SLC30A8
    nsv6854327copy number variation1nstd229human GRCh38 chr8: 117,175,785-117,176,122 , GRCh37.p13 chr8: 118,188,024-118,188,361 LOC105375716, SLC30A8
    nsv6853736copy number variation1nstd229human GRCh38 chr8: 116,995,601-117,006,100 , GRCh37.p13 chr8: 118,007,840-118,018,339 SLC30A8
    nsv6853252copy number variation1nstd229human GRCh38 chr8: 117,167,103-117,167,146 , GRCh37.p13 chr8: 118,179,342-118,179,385 LOC105375716, SLC30A8
    nsv6852881copy number variation1nstd229human GRCh38 chr8: 117,037,939-117,038,271 , GRCh37.p13 chr8: 118,050,178-118,050,510 SLC30A8
    nsv6852831copy number variation1nstd229human GRCh38 chr8: 116,993,164-116,995,928 , GRCh37.p13 chr8: 118,005,403-118,008,167 SLC30A8
    nsv6851863copy number variation1nstd229human GRCh38 chr8: 117,154,139-117,159,716 , GRCh37.p13 chr8: 118,166,378-118,171,955 LOC105375716, SLC30A8
    nsv6851586copy number variation1nstd229human GRCh38 chr8: 116,993,101-116,994,900 , GRCh37.p13 chr8: 118,005,340-118,007,139 SLC30A8
    nsv6850583copy number variation1nstd229human GRCh38 chr8: 117,059,301-117,064,800 , GRCh37.p13 chr8: 118,071,540-118,077,039 SLC30A8
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