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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5322525inversion1nstd204human GRCh37.p13 chr7: 65,776,458-71,393,640 , GRCh38.p13 chr7: 66,311,471-71,928,655 , SKP1P1, 64 more genes
    nsv5117071mobile element insertion1nstd203human GRCh38 chr7: 66,421,657-66,421,672 , GRCh37.p13 chr7: 65,886,644-65,886,659 SKP1P1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4563011sequence alteration1nstd166human GRCh37.p13 chr7: 65,872,400-66,347,293 , GRCh38.p12 chr7: 66,407,413-66,882,306 SKP1P1, RABGEF1, 15 more genes
    nsv4524163copy number variation1nstd166human GRCh37.p13 chr7: 65,832,999-65,942,000 , GRCh38.p12 chr7: 66,368,012-66,477,013 SKP1P1, LINC00174, 3 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4366482copy number variation2nstd173human GRCh37 chr7: 65,882,671-65,930,368 , GRCh38.p12 chr7: 66,417,684-66,465,381 LOC729126, SKP1P1
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4145621copy number variation1nstd166human GRCh37.p13 chr7: 65,886,356-65,893,697 , GRCh38.p12 chr7: 66,421,369-66,428,710 SKP1P1
    nsv3961165copy number variation1nstd168human GRCh38 chr7: 66,363,820-66,434,957 , GRCh37.p13 chr7: 65,828,807-65,899,944 LOC729126, GTF2IP9, 2 more genes
    nsv3923928copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 62,074,825-65,951,097 , GRCh37 chr7: 62,437,390-66,313,662 , GRCh38 chr7: 62,977,012-66,848,675 ASL, ERV3-1, 153 more genes
    nsv3923428copy number variation1nstd102humanPathogenic GRCh38 chr7: 64,657,050-72,243,063 , NCBI36 chr7: 63,754,863-71,345,984 , GRCh37 chr7: 64,117,428-71,708,048 LOC402279, LOC101929322, 112 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3917508copy number variation1nstd102humanPathogenic GRCh37 chr7: 62,196,742-75,061,986 , GRCh38 chr7: 62,736,364-75,432,710 , NCBI36 chr7: 61,834,177-74,899,922 GTF2IP4, ZNF680P1, 285 more genes
    nsv3916763copy number variation1nstd102humanLikely benign GRCh38 chr7: 65,835,271-66,837,033 , GRCh37 chr7: 65,300,258-66,302,020 , NCBI36 chr7: 64,937,693-65,939,455 LOC84214, LOC346329, 27 more genes
    nsv3915165copy number variation1nstd102humanPathogenic GRCh38 chr7: 62,570,287-67,823,956 , NCBI36 chr7: 61,668,100-66,926,378 , GRCh37 chr7: 62,030,665-67,288,943 VN1R34P, GTF2IP14, 169 more genes
    nsv3915047copy number variation1nstd102humanPathogenic GRCh37 chr7: 53,341,752-68,041,200 , NCBI36 chr7: 53,309,246-67,679,136 , GRCh38 chr7: 53,274,059-68,576,213 VN1R25P, SNORA22C, 333 more genes
    nsv3913119copy number variation1nstd102humanPathogenic NCBI36 chr7: 62,074,898-74,882,566 , GRCh38 chr7: 62,977,085-75,415,352 , GRCh37 chr7: 62,437,463-75,044,630 ARAFP1, WBSCR23, 285 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MNX1-AS2, VN1R31P, 2682 more genes
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