akip1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	AKIP1, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	AKIP1, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	AKIP1, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	AKIP1, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	AKIP1, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	AKIP1, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	AKIP1, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	AKIP1, SDHCP4, 620 more genes
nsv3912558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865	AKIP1, TRIM22, 546 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	AKIP1, MTND5P21, 506 more genes
nsv4350476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589	AKIP1, KRTAP5-3, 457 more genes
nsv3919565	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092	AKIP1, OR51A7, 437 more genes
nsv3892294	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-9,704,511 , GRCh38.p12 chr11: 230,615-9,682,964	AKIP1, MRPS24P1, 405 more genes
nsv3902973	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 6,969,013-9,257,231 , GRCh38.p12 chr11: 6,947,782-9,235,684	AKIP1, NLRP14, 55 more genes
nsv3893825	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 8,691,402-8,933,010 , GRCh38.p12 chr11: 8,669,855-8,911,463	AKIP1, SNORA3A, 7 more genes
nsv3923443	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 7,973,799-10,415,328 , GRCh37 chr11: 8,017,223-10,458,752 , GRCh38 chr11: 7,995,676-10,437,205	AKIP1, TMEM41B, 51 more genes
nsv3901627	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 7,837,338-9,295,428 , GRCh38.p12 chr11: 7,815,791-9,273,881	AKIP1, DENND2B, 37 more genes
nsv4675904	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 8,859,352-9,226,956 , GRCh38.p12 chr11: 8,837,805-9,205,409	AKIP1, DENND2B, 12 more genes
nsv3906470	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 8,902,282-9,200,052 , GRCh38.p12 chr11: 8,880,735-9,178,505	AKIP1, ASCL3, 11 more genes

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