cass4[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3890099	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 55,015,531-55,018,532 , GRCh38.p12 chr20: 56,440,475-56,443,476	CASS4
nsv3904664	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 55,017,124-55,018,532 , GRCh38.p12 chr20: 56,442,068-56,443,476	CASS4
nsv3918295	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 54,594,888-58,190,583 , NCBI36 chr20: 52,644,834-56,199,045 , GRCh37 chr20: 53,211,427-56,765,639	CASS4, MTRNR2L3, 59 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	CASS4, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	CASS4, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	CASS4, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	CASS4, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	CASS4, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	CASS4, FTLP1, 472 more genes
nsv6112778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273	CASS4, LINC01742, 253 more genes
nsv3911673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321	CASS4, LOC105372709, 226 more genes
nsv4357849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528	CASS4, RBM38, 192 more genes
nsv3894116	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202	CASS4, ATP5F1E, 254 more genes
nsv3910223	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 51,286,111-62,385,999 , GRCh37 chr20: 51,852,704-62,915,555 , GRCh38 chr20: 53,236,165-64,284,202	CASS4, ATP5F1E, 253 more genes
nsv3912982	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207	CASS4, ATP5F1E, 103 more genes
nsv6311086	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459	CASS4, CTSZ, 75 more genes
nsv3910818	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167	CASS4, RNA5SP481, 855 more genes
nsv7148186	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667	CASS4, LOC105372717, 245 more genes
nsv6637604	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 52,517,925-55,402,822 , GRCh38.p12 chr20: 53,901,386-56,827,766	CASS4, DOK5, 34 more genes
nsv3901084	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 54,541,125-55,162,415 , GRCh38.p12 chr20: 55,966,069-56,587,359	CASS4, FAM209B, 13 more genes

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Items: 20

Number of Variants: 20

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