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Items: 1 to 20 of 1679

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4679145copy number variation1nstd189human GRCh38.p12 chr1: 104,355,881-105,254,869 , GRCh37.p13 chr1: 104,898,503-105,797,491 LOC105378880
    nsv4680501copy number variation1nstd189human GRCh38.p12 chr1: 104,355,881-105,239,921 , GRCh37.p13 chr1: 104,898,503-105,782,543 LOC105378880
    nsv4680159copy number variation1nstd189human GRCh38.p12 chr6: 80,872,522-81,589,859 , GRCh37.p13 chr6: 81,582,239-82,299,576 LOC105377871
    nsv4679249copy number variation1nstd189human GRCh38.p12 chr4: 62,720,179-63,265,520 , GRCh37.p13 chr4: 63,585,897-64,131,238 EXOC5P1
    nsv4679064copy number variation1nstd189human GRCh38.p12 chr13: 55,660,500-56,122,139 , GRCh37.p13 chr13: 56,234,635-56,696,273 HNF4GP1
    nsv4679007copy number variation1nstd189human GRCh38.p12 chr10: 55,175,524-55,593,335 , GRCh37.p13 chr10: 56,935,284-57,353,095 PCDH15
    nsv4680638copy number variation1nstd189human GRCh38.p12 chr9: 24,133,723-24,540,423 , GRCh37.p13 chr9: 24,133,721-24,540,421 LOC105375994
    nsv4680389copy number variation1nstd189human GRCh38.p12 chr1: 175,460,875-175,862,414 , GRCh37.p13 chr1: 175,430,011-175,831,550 TNR
    nsv4679688copy number variation1nstd189human GRCh38.p12 chr1: 190,818,438-191,173,185 , GRCh37.p13 chr1: 190,787,568-191,142,315 HNRNPA1P46
    nsv4680502copy number variation1nstd189human GRCh38.p12 chr1: 175,460,875-175,798,492 , GRCh37.p13 chr1: 175,430,011-175,767,628 TNR
    nsv4681004copy number variation1nstd189human GRCh38.p12 chr1: 175,461,076-175,793,886 , GRCh37.p13 chr1: 175,430,212-175,763,022 TNR
    nsv4679646copy number variation1nstd189human GRCh38.p12 chr1: 175,461,076-175,791,616 , GRCh37.p13 chr1: 175,430,212-175,760,752 TNR
    nsv4679373copy number variation1nstd189human GRCh38.p12 chr1: 175,459,438-175,788,812 , GRCh37.p13 chr1: 175,428,574-175,757,948 TNR
    nsv4679463copy number variation1nstd189human GRCh38.p12 chr1: 175,460,875-175,786,090 , GRCh37.p13 chr1: 175,430,011-175,755,226 TNR
    nsv4680620copy number variation1nstd189human GRCh38.p12 chr1: 175,467,396-175,791,616 , GRCh37.p13 chr1: 175,436,532-175,760,752 TNR
    nsv4680257copy number variation1nstd189human GRCh38.p12 chr1: 175,467,396-175,783,601 , GRCh37.p13 chr1: 175,436,532-175,752,737 TNR
    nsv4680689copy number variation1nstd189human GRCh38.p12 chr4: 27,070,916-27,377,454 , GRCh37.p13 chr4: 27,072,538-27,379,076 LINC02261
    nsv4679362copy number variation1nstd189human GRCh38.p12 chr6: 161,902,492-162,197,683 , GRCh37.p13 chr6: 162,323,524-162,618,715 PRKN
    nsv4680363copy number variation1nstd189human GRCh38.p12 chr8: 128,272,106-128,557,818 , GRCh37.p13 chr8: 129,284,352-129,570,064 LINC00824
    nsv4679908copy number variation1nstd189human GRCh38.p12 chr21: 21,364,416-21,644,901 , GRCh37.p13 chr21: 22,736,736-23,017,222 NCAM2
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