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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564225copy number variation1nstd102humanUncertain significance GRCh37 chr16: 17,451,859-17,451,917 , GRCh38.p12 chr16|NW_019805500.1: 359,263-359,321 , GRCh38.p12 chr16: 17,358,002-17,358,060 XYLT1
    nsv4456700copy number variation1nstd102humanUncertain significance GRCh37 chr16: 17,193,610-17,469,499 , GRCh38.p12 chr16: 17,099,753-17,375,642 , GRCh38.p12 chr16|NW_019805500.1: 101,014-376,903 XYLT1, LOC102723692
    nsv6309850copy number variation1nstd102humanUncertain significance GRCh37 chr16: 17,202,552-17,451,927 , GRCh38.p12 chr16: 17,108,695-17,358,070 , GRCh38.p12 chr16|NW_019805500.1: 109,956-359,331 XYLT1, LOC102723692
    nsv3871211copy number variation1nstd102humanPathogenic GRCh37 chr16: 17,202,532-17,564,673 , GRCh38 chr16: 17,108,675-17,470,816 XYLT1, LOC105371106, 2 more genes
    nsv5672920copy number variation1nstd102humanPathogenic GRCh37 chr16: 17,564,281-17,564,653 , GRCh38.p12 chr16: 17,470,424-17,470,796 , GRCh38.p12 chr16|NW_019805500.1: 471,685-472,057 XYLT1, LOC105371106, 1 more genes
    nsv3924438copy number variation1nstd102humanLikely benign GRCh37 chr16: 17,263,657-18,060,317 , NCBI36 chr16: 17,171,158-17,967,818 , GRCh38 chr16: 17,169,800-17,966,460 XYLT1, LOC107987234, 3 more genes
    nsv3904093copy number variation1nstd102humanLikely benign GRCh37 chr16: 16,895,835-17,505,309 , GRCh38.p12 chr16|NW_019805500.1: 1-412,713 , GRCh38.p12 chr16: 16,801,978-17,411,452 XYLT1, LOC102723692, 2 more genes
    nsv3915907copy number variation1nstd102humanUncertain significance NCBI36 chr16: 17,229,662-17,602,435 , GRCh37 chr16: 17,322,161-17,694,934 , GRCh38 chr16: 17,228,304-17,601,077 XYLT1, LOC107987234, 1 more genes
    nsv6291624copy number variation1nstd102humanUncertain significance GRCh37 chr16: 16,837,614-17,371,034 , GRCh38.p12 chr16: 16,743,757-17,277,177 , GRCh38.p12 chr16|NW_019805500.1: 1-278,438 XYLT1, SPRING1P3, 2 more genes
    nsv6637585copy number variation1nstd102humanUncertain significance GRCh37 chr16: 16,955,593-17,467,141 , GRCh38.p12 chr16|NW_019805500.1: 1-374,545 , GRCh38.p12 chr16: 16,861,736-17,373,284 XYLT1, SPRING1P3, 2 more genes
    nsv3920014copy number variation1nstd102humanUncertain significance GRCh37 chr16: 16,955,362-17,462,387 , NCBI36 chr16: 16,862,863-17,369,888 , GRCh38 chr16: 16,861,505-17,368,530 XYLT1, SPRING1P3, 2 more genes
    nsv3916649copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,760,627-18,687,298 , GRCh37.p13 chr16: 14,853,126-18,779,797 , GRCh38.p12 chr16: 14,759,269-18,768,475 , GRCh38.p12 chr16|NT_187607.1: 293,011-2,659,700 XYLT1, RRN3, 90 more genes
    nsv3920316copy number variation1nstd102humanPathogenic GRCh38 chr16: 14,816,348-18,658,403 , NCBI36 chr16: 14,817,706-18,577,226 , GRCh37 chr16: 14,910,205-18,669,725 XYLT1, MIR6511A1, 82 more genes
    nsv3904576copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,318,664-18,778,064 , GRCh38.p12 chr16: 15,224,807-18,766,742 XYLT1, RPL7P47, 58 more genes
    nsv3923793copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,141,934-18,577,226 , GRCh37 chr16: 15,234,433-18,669,725 , GRCh38 chr16: 15,140,576-18,658,403 XYLT1, LOC102723692, 62 more genes
    nsv3921429copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,917,806-18,149,685 , GRCh38 chr16: 14,823,949-18,055,828 , NCBI36 chr16: 14,825,307-18,057,186 XYLT1, NOMO1, 61 more genes
    nsv3922278copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,910,205-18,141,051 , GRCh38 chr16: 14,816,348-18,047,194 , NCBI36 chr16: 14,817,706-18,048,552 XYLT1, MIR6770-1, 61 more genes
    nsv3904490copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,316,618-18,181,971 , GRCh38.p12 chr16: 15,222,761-18,088,114 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 XYLT1, NDE1, 37 more genes
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 XYLT1, MIR484, 37 more genes
    nsv4729445copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,375,911-18,198,455 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,282,054-18,104,598 XYLT1, BMERB1, 38 more genes
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